“World’s most addictive and widely used drug”

By Macsylver on Monday 13 February 2017 08:36 - Comments (17)
Category: Microscope, Views: 5.615


Almost everyone is familiar with caffeine, and most of us have taken it with or without knowing it. Foods containing caffeine often go unrecognised, making the task of limiting intake of the stimulant challenging. But have you ever wondered about how caffeine would look underneath a microscope? Of course your question at the time taking for example your cup of coffee would have been “will it help me through the day?”

Generally, most people assume that hard drugs like cocaine, heroin, nicotine are the most addictive of their kind when in fact, they aren’t. While the addictive properties in these drugs are intense, potency isn’t the only factor that plays into addiction; availability and frequency of use are important too.

When caffeine enters the brain, Dopamanergic signaling from midbrain regions like the ventral tegmentum area are responsible for this “do it again” signal. Caffeine indirectly causes the release of dopamine, but the pleasure effect comes from the indirect release of opioids caused by neurons with dopamine receptors.

So why take micrographic pictures of caffeine? The idea of these micrographs came from the same idea as described this early publication you can read here: “Crystals that will ease your pain”. While elaborating further on this idea I created several more micrographs of medicine, drugs, food adjectives and even tears. And since caffeine is a widely used (natural) substance that is also used as a food Adjective, it came natural too also add its results to the project.

The First results
This image is the result of the first try of crystallising 100% caffeine powder. The Caffeine powder was added to demineralised water and heated in a water bath to 100°C. After this first step large drops of the sample where placed on a slide, within 45minutes the drops where fully crystallised and ready be imaged.

Caffeine crystals; formed out of 100% caffeine powder dissolved in demineralised water, made visible by using a cross polarised light microscope with an Berek filter.

The large image above is a shot made out of 25+ images, these images where shot in a comprehensive grid covering only a part of the sample. The images where later stitched together in digital post production. The total resolution of the image above is about 100+ mega pixels. Below a cropped (100%) part of the image showing you the beautiful details, structures & colours of the crystals that where formed by the caffeine.

Caffeine crystals; formed out of 100% caffeine powder dissolved in demineralised water, made visible by using a cross polarised light microscope with an Berek filter. (100% zoom of above image)

So next time you take one of the world’s most addictive drug, envision this microscopic molecule working its magic in your body.

“Crystals that will ease your pain!”

By Macsylver on Wednesday 8 February 2017 19:02 - Comments (16)
Category: Microscope, Views: 2.756

Almost everyone is familiar with painkillers, and most of us have taken them. But have you ever wondered about how they would look underneath a microscope? Of course your question at the time taking that painkiller would have been “will it ease my pain?”

There are a large number of painkillers available from the weakest aspirin to the strongest oxymorphone. Each works in a different way. Most people only need to take painkillers for a few days or weeks at most, but some people need to take them for a long time.

Painkillers can be taken by: mouth as liquids, tablets, or capsules, by injection, or via the rectum for example, suppositories. And some are even available as a creams or an ointment.

So why take micrographic pictures of pain medication?
Behind every used painkiller there is a story. Stories of the people taking their pain medication, but most of these stories are of course no happy stories. One day a few years back, I did not have a happy story, and I was bound for a long time taking strong pain medication.

During this period I was not really able to do my normal photography work. So I found back some old moleskins, and went trough all my notes. One think popped-up several times “Micrographs”. Combining my “two” passions; science and photography.

As an licensed medical laboratory analyst, I saw lots of beautiful things underneath the microscope when I was working at the RIVM. Capturing these moments in a form of art was always a wish.

So I started to build a setup that would enable me to go back to this “happy place”. Getting to know the world in a different way, by using things we “consume” in our “daily” life, but putting them underneath a microscope. Creating images “from another world” with a different perspective. Where structures, shapes, patterns, details, colours an many other things will (hopefully) make you look astonished.

After a lot of research about possibilities (within the available budget), I found my starting setup. A Novex B microscope that was able to show me some of the worlds within microscopy.

By “modding” this microscope I could use the techniques like; bright-field, cross polarised, dark-field, phase contrast and oblique illumination.

A few weeks later the setup arrived, and the first thing that popped-up in my mind, was to try and see if I can make the medicine I was taking visible. But unfortunately that first step of making the particular medication visible by trying to crystallise it failed.

So where to start?
Like the introduction almost everyone has taken some painkillers in there life, so we can all relate to these medicine. The most common OTC (over the counter) pain medications are aspirin, acetaminophen, ibuprofen, diclofenac & naproxen. So starting with these 5 painkillers would be a good start.

The First results
In the last months I have been experimenting allot to get the best results in therms of how to crystallise and capture these 5 OTC pain medications. I can happily report that I have managed to get beautiful micrographs of aspirin, acetaminophen & diclofenac.

Diclofenac crystals after waiting for 72 hours, made visible by using a cross polarised light microscope.

Diclofenac crystals after waiting for 72 hours, made visible by using a cross polarised light microscope. (100% zoom of above image)

Acetaminophen crystals after waiting for 3 hours, made visible by using a cross polarised light microscope.

Acetaminophen crystals after waiting for 3 hours, made visible by using a cross polarised light microscope. (100% zoom of above image)

Aspirin crystals after waiting for 1 hour, made visible by using a cross polarised light microscope.

Aspirin crystals after waiting for 1 hour, made visible by using a cross polarised light microscope. (100% zoom of above image)

Work in progress:
Hopefully in the future I will be able to make ibuprofen & naproxen visual. This so my goal of having an exposition with these OTC pain medications can be realised, among the other legal and non-legal medication I would love to categorise and make visual.

So next time you take one of the world’s most popular painkillers aspirin, diclofenac or acetaminophen, envision this microscopic molecule working its magic in your body.

How do tears turn into art?

By Macsylver on Friday 3 February 2017 19:41 - Comments (0)
Category: Microscope, Views: 1.726

In the previous two blogs I gave a glimpse of what Micrograph Stories is partly about. Before I continue writing about previous and upcoming project details, ideas and future plans, I want to share this TEDx talk. A talk about my project Micrograph Stories & Imaginarium of Tears.

A TED talk at TEDxAmsterdam about Imaginarium of Tears. "How do tears turn in to art?"

With this blogpost, I hope to give you a bit more basic insights on who I'm and how Micrograph Stories and Imaginarium of Tears evolved to what it's today.

Micrography and the online drug trade.

By Macsylver on Tuesday 24 January 2017 12:30 - Comments (17)
Category: Microscope, Views: 3.116

Introduction visuals and story on The Dutch TV NPO; De kennis van nu - De harddrugs van Dr. Mikkers

How Micrography sparked my interest in the evolving online drug trade.

While working on the project Micrographic Stories new ideas swiftly surfaced after starting the initial project of visualising (OTC) painkillers. The project quickly expanded toward a wider spectrum of “daily” consumed (prescription) medicine and foods additives. Because some (hard) drugs are closely related to prescription medicine, the topic of visualising hard drugs was quickly raised. To elaborate on this idea and concept of visualising drugs underneath the microscope, I needed to get my hands on different kinds of drugs.

After some research, one of my acquaintances told me that getting drugs from the street was “old fashioned” these days. He said:
“Most (young) people these days get their Ecstasy, MDMA or other hard drugs by going online. Just google how to get on Agora by using TorBrowser. The quality, price, service and ‘entry level’ made it better, easier and most important ‘safer’ than getting your drugs on the corner of the street from some random guy.”
Bitcoin and the deep web were not subjects new to me when starting this project. During my first year of study (2007) at the Royal Art Academy (I/M/D department) in The Hague, a lecture was given about the deep web (invisible web). Part of this lecture was to explore, discuss, gain knowledge and understand the basics and possibilities of the deep web. At that time it was not as advanced, easy, safe and fast as today’s deep web, but it was still fascinating. A few years later Bitcoin was upcoming, and lectures were spent on crypto currency, getting me to mine my own Bitcoins. But at that time I did not see the direct (security) potential of Bitcoin, or of using it to buy things in the Deep Web.

Five minutes after using Google Search, I was browsing Agora on The Deep Web with my TorBrowser. Surprisingly things had changed a lot in the past years, websites were faster, easier to find and the user experience was better compared to the “invisible web” experience from 2007.

After looking around on Agora, I decided to make my first purchase to see if it would actually work as advertised. By transferring a small amount of my Bitcoin from my local wallet to my Agora wallet, I was ready to buy the lowest amount of MDMA possible, since I needed less than 0.1 gram to make my dilutions.

Agora displayed search results on MDMA, rendered by the TorBrowser.

I started searching on Agora for MDMA. Within seconds it gave me a list of items and its vendors. The vendor from The Netherlands who was advertising with the smallest amount of 0.3 grams and 84% purity was the one I decided to go with, costing me 0.06198347 BTC.
1BTC equals 213,56 Euro, so this purchase would cost me 13,24 Euro.
Vendor / product page on Agora. Selling 0.3gram of 84% pure MDMA

I gathered up the confidence to purchase the MDMA based on good reviews and ratings that were given by others, such as:
“Fast delivery and great stealth, good communication with vendor and products look really good !!!! Will order again !!!! Truste”
The envelope that was received after 2 days.

Two days later an envelope of “the Rotterdam School of Management” came through the mail (a fake, home printed envelope). At first I thought it had been a wrong delivery, but it had the exact information and alias on it as provided through Agora using PGP encryption. Surprised and confused at the same time, I opened the envelope.

Behind the letter a thick stack of empty graphical paper was included. The cut out was to hold the pony pack with the ordered 0.3grams of MDMA crystals in place.

It was now time to take the next step in this project.
By using a few µg of MDAM I started creating the slides, by dissolving the crystals in demineralised water. The solution was later used to create several drops of 1 to 5 µl on a slide, hoping these drops would crystallise in time. When fully dried and crystallised the slide was ready to be imaged underneath the cross polarisation microscope. Lucky as I was, one of the drops crystallised perfectly and generated an amazing result!

MDMA Crystals ∅ Cross polarisation microscope with 200x enlargement. ⿻ overview

∢ MDMA Crystals ∅ Cross polarisation microscope with 200x enlargement. ⿻ 100 % crop

Happy with the result, it was time to properly dispose of the MDMA.
Together with some old expired medicine, I handed in a small plastic bag at the local pharmacy. Wanting to make sure the MDMA would be properly discarded, because flushing, selling or providing to others was not a legit option to me.

Walking out of the pharmacy my brain was in a twist. “I broke the law by buying and being in possession of a hard drug.” Struggling with this fact I asked myself if I should continue this project, and accept any possible risks involved; knowing that there is a tolerance policy in The Netherlands on possession of hard drugs in small quantities. For example:
“One globule, one ampoule, a wrapper, a pill / tablet (in each case, a detected amount of up to 0.5 grams); a consumption unit of 5 ml GHB is quantified as personal use”
So in this case I would not be likely to be persecuted or arrested. But what would happen if I made a habit out of using The Deep Web and Bitcoin, purchasing hard drugs to support my project? On the way home the question that kept repeating in my mind was:
Should I order another drug, and continue this project??
∢ LSD Crystals ∅ Cross polarisation microscope with 40X enlargement. ⿻ overview

∢ LSD Crystals ∅ Cross polarisation microscope with 200x enlargement. ⿻ 100 % crop

Scrolling down and seeing another micrograph of drugs gave away the answer to the question if I should order another drug.
Yes, my curiosity and vision behind this project was bigger. Bigger than my initial concerns about purchasing and possessing very small amounts of hard drugs. Next to that, the result of the first drug visualisation of MDMA got me “hooked” on the beauty of its microscopic; crystals, structures and colours.

I had seen a lot of crystallisation processes happening under the microscope in the last year and this was with no doubt one of the most vivid, intense and mind blowing results I had encountered. Stopping was not an option anymore; I got “addicted” and obsessed with documenting crystalline formations of drugs. So to expand the series I started to use the same method and process as I used for MDMA.

Luck was on my side for a long time; by making small adjustments to my experiments crystallising new drugs was never far away from giving me new and beautiful results. LSD, GHB, DMT, Amphetamine and 2CB they all gave results I had thought were never possible in the first place. They kept me wondering about how it’s possible that these microscopic structures can look this beautiful and diverse underneath a microscope. Giving me even more drive to share its beauty with the world.

Not only good and useful results where achieved. From all the things that where purchased along the way I could not create crystalline formations of Cocaine, Ketamine and Oxycodone. As frustrating as it got I decided not to actively continue the exploration and visualisations of these and other new drugs. So for the moment I’m only able to present you these micrographs, maybe in the future I’m able to restart this part of the project with the help of others.

∢ GHB Crystals ∅ Cross polarisation microscope with 100X enlargement. ⿻ overview

∢ GHB Crystals ∅ Cross polarisation microscope with 100x enlargement. ⿻ 100 % crop

So why am I making these micrographs (of hard drugs)?
By creating this micrographic art, I want to show the microscopic structures and create more awareness about daily consumed products. Most of us tend not to consume (hard) drugs, but other products, as in: painkillers or (prescription) medication or even food additives are more commonly consumed, and more familiar. For example:
At the first sign of a headache, most of us pop pills without hesitation. We get on with it, satisfied that medicine will see us through.
We often use products without hesitation. Who these days is actually reading every medication leaflet or product label? Some of us are very involved and aware about there product use, others “don’t care about what’s actually inside” until things may go wrong. Involved or not the things inside are often abracadabra to us.

By giving you a different angle (in this case a microscopic image) you might become more interested about the workings of these products and their “active ingredients” that may be in there for the better or for the worse.

To give an example about how I think this might work: Everyone is familiar with soda drinks. Many of these drinks nowadays have a light version that tends to be “healthier” than the regular one. Containing not sugar but aspartame. The aspartame is used as a substitute for sugar, and can actually be more harmful. It has been linked to almost a hundred different health problems. To raise awareness about aspartame I would try to visualise aspartame as the food additive itself. By doing this in a vivid and impressive way I’m hoping to gain your attention and along the way I might be able to teach you a bit more about aspartame, its use and therefore maybe its dangers.

∢ DMT Crystals ∅ Cross polarisation microscope with 400x enlargement. ⿻ overview

∢ DMT Crystals ∅ Cross polarisation microscope with 400x enlargement. ⿻ 100 % crop

But If your goal is to create awareness and involvement with the products we consume, then why are you sharing information about purchasing drugs on the deep web?
While working on this project I kept sharing my results, to the point of creating a “work in progress page”. By doing this I was able to gain feedback, interact and gain more information about how my Micrographs and Micrographic stories where received.

By sharing information about the project, people became interested about also my personal involvement with drugs and how I got my samples. Quite often questions like: Are you using yourself? or How do you get your samples? where asked.
“No, I have never experimented with hard drugs myself and the Micrographs of drugs that are displayed here are bought by using The Deep Web.”
The first part of the answer always let to the explanation of my concept and vision as explained above. Most of the time this explanation gave them a clear understanding and a deeper bond with my work.

As for the second part of my answer things where not so clear. In general most people did not know that it was even possible to order drugs “online” and getting them delivered at home. They where very surprised, and sometimes even shocked about the possibilities and not knowing that there is a “market space like E-bay” on The Deep Web selling drugs a.o. legal and illegal things.

By sharing my Deep Web experience I hope create awareness towards The Deep Web. Of course The Deep Web is more then only an illegal online place where you can order dugs with full anonymity and pay with Bitcoin. If this Dark Web is new to you?! I hope by sharing this information it will trigger you to do some more research. Once you do understand the pro’s and cons of this fascinating evolving online service, we can then identify problems together. Starting a discussion about how to handle these situations accordingly.

∢ Amphetamine Crystals ∅ Cross polarisation microscope with 40X enlargement. ⿻ overview

∢ Amphetamine Crystals ∅ Cross polarisation microscope with 40X enlargement. ⿻ 100 % crop

Future progress:
The next step in this project would be to continue the exploration of different not yet imaged types of “daily” consumed (prescription) medicine, foods additives and (hard) drugs, extending the series of micrographs that are already made. Ideal it would be to collaborate with institutes, companies organisations or schools hat support these Visualisations. By combining Art & Science we are hopefully able to generate more awareness and start an more open conversation about these subjects by using micrographs.

Please feel free to contact me if you have any suggestions, questions, comments, feedback or are willing to support or collaborate on this project.

∢ 2C-B Crystals ∅ Cross polarisation microscope with 200x enlargement. ⿻ overview

∢ 2C-B Crystals ∅ Cross polarisation polarisation microscope with 200x enlargement. ⿻ 100 % crop

Turning an 30+ year old microscope into a more modern microscope.

By Macsylver on Thursday 19 January 2017 01:41 - Comments (17)
Category: Microscope, Views: 3.958

Current Microscope Setup with the DIY scanning stage hardware and software.


In the beginning of this year (2016) I bought a new microscope, but not just one. I bought the Nikon TMD Inverted DIC microscope a micro-scope made in the mid 1980’s. The decision for this microscope was made after doing quite some research. Research on different types of light microscopes that were able to compete with my “wish list” (DIC, camera mounting port, good optics, good brand, proved techniques, locally available and within budget) But why did I end up choosing for this particular microscope thats was made in the mid 1980's?

The Images from the original Nikon TMD Inverted microscope. More technical information can be found in these PDF’s: Standard TMD, DIC and Epi Fluorescence.

If you followed the four links above, you may have seen that this microscope was specially made for photomicrography on 35mm (full-frame) camera’s and had a second view port for other (film) camera’s. Something that is I think still very unique these days, making it a “perfect candidate” to connect a digital full frame camera.
The Diaphot microscope was designed for photo micrography, with photographic capability built into the optical system. The optical design utilises a built-in binocular body, inclined at 45 degrees, and only one reflecting surface in the microscope body to reduce reflections and glare and maximise image contrast.
What also makes is special is that it it comes with DIC optics (something that is very hard to get your hands on for a microscope in this “league” and budget). Next to that it was locally available at a trustworthy vendor. So I decided to go there to check it out, since you can only make such a final decision by actually using and testing it in a real life situation. Testing it with your own slides, and see if it would really be the ideal new workhorse.

From the moment I walked into the shop seeing the microscope, I was sold! What a beautiful piece of equipment! And I It got even more excited when I started using it. The ergonomics were perfect (especially cause it was inverted which gave me a lot of working space), it was very stable due its heavy duty materials and the optics and were stunning compared with my other microscope. I was sold by its “power” and buying the microscope was only one step away, I only needed to check one more important thing; Will it take better images than my other microscope that I’m currently using.

So I grabbed my Canon 5D MKIII camera and the Nikon to Canon mount converters, but unfortunately the mount converters did not fit. This was because the photo mount assembly on the microscope, had a special overhang and mount addition to it, to be able to hold the older (analog) Nikon cameras camera better in place. Since I’m a Canon user the camera could not be connected without any of these mount converters, therefore I was not able test the optical quality of the microscope by taking images.

Desperate as I was, (since I really wanted to buy this beauty) I started looking at some available options and solutions regarding the mount. After a few minutes I found out that the photo mounting assembly could be fully removed from the microscopes body, leaving only a big cap by removing some screws! This would mean that I could put and hold the camera tightly in front of the gap of the microscope to see if it would give me some results.

Within the next few minutes the photo mount assembly of the microscope was removed. Meaning I could manually hold the Canon camera in front of the big round gap that was left in the microscopes body. It payed of, the first images came out crystal clear. It surprised me that a “dirty fix” like this gave me already such bright and sharp images.

Would this mean that if I buy a canon lens mount and attach it to the microscope’s body, that the problem would be fixed? Or could I in some way get rid of the overhang and mount additions on the Nikon microscope photo mount assembly?

Eventually I went for the last option since the vendor agreed to help out and mill away the steel overhang / mount additions on the lathe. This irreversible procedure would not compromise the mount in any way, plus in this way it was also possible to connect other digital camera’s. Meaning it would have “more value” and keeping its original parts, with only some limited adjustments that would improve its use.

Crop from an image on the web showing the original mount

The milled version on my microscope mount.

Since I did not expect to write a full post on this, good imagery documentation is not always available, so images of the microscopes original state and process made along the way is not always available. But I will try to explain all as good as I can, so others can maybe go and take the same road with this or other microscopes.

On the left in the image you see quite some black overhang and support on the ring around the mount. On the right you see that the Nikon mount is removed and that the black overhang and support is milled away up to the construction. This was needed so it could fit any other camera mount in the future. In this case the big holes are there to remove the mount assembly from the microscope. The smaller screw holes are there to connect any lens mount.

After milling away the “overhang” and reconnecting it back to the microscope we reattached the Nikon to Canon mount adapter. “Surprisingly” it was now possible to connect the Canon 5D MK III to the microscope. It was now time to take some “real images” and see its power projected on a digital full frame camera, Stunning micrographs popped up on the screen of my laptop one after another without any problems.

At that point my wish list was (almost) complete DIC optics √, working camera mounting √, good overal optics √, inverted √, well known microscope type and brand √, Good ergonomics √, locally available √, well tested √ and within budget √.

It had all I could wish for and extra, accept for a scanning stage. But as most microscope owners know getting a scanning stage that can be precisely controlled by a computer to take images at every step is hard to come by. If it exists or is available for your (type of) microscope its often very expensive and not within our budget.

But since it had “all” I wanted and I expected that the scanning stage was not an option by far in my budget or available second hand. I decided to buy it and mod & tweak it later on myself. Since I had the strong believe that this would work with this microscope and its standard stage.

Now a few months later I’m proudly presenting my first finished version of the microscope additions, mods and its digital photo scanning stage addition. Since there were some hardware and software iterations along the road in the past months, I will only show you the “final” working result and used parts for now. Below you will find some more information about final results and some information about why I need a digital photo scanning stage and how it works, together with some future plants for it.

The goals I had with this new setup and its modifications is to get more functions, a better work flow, time reduction, higher resolution pictures and a smaller error mage in the images. To do this I needed to build a digital photo scanning stage.

A (digitally controlled photo) scanning stage is a microscope stage were its hardware can be controlled by software to get consistent precision movements in terms of a few microns or a time. By being able to control with such precision you can generate high resolution images. With each step made, images are taken using high power magnifications objectives to index (photograph) the specimen on the slide. This ensures the highest detail able to be captured, but because you are zoomed in so far its not possible to see the whole specimen. Therefore you need to “scan” the specimen in a comprehensive grid until you covered the whole specimen.

A simple example of a comprehensive grid imaging example, having 10 X axis rows and 10 Y axis column resulting in 100 images that need to be stitched together.

This is the most simple way not including any redundancy into the imaging of the specimen. For example if you would bump against foto number 43 and 76 you would have 2 big blurry parts with no “error correction” therefore I calculated 1/3 of overlap on each side so every part of the specimen will be photographed and seen on 3 different images.

To do this you need to control its hardware with software the fancier you make and program the software, the more options and error correction you will have on controlling the hardware. In my case it only controls the step motors on the X and Y axis of the table and triggers the camera accordingly.

Depending on the magnification of the objective you are using you can choose a “calibrated” step size that fits the lens magnification. Calibrated means that we know how many steps the step motor has to take to get a fully new part of the specimen in frame. By dividing these step numbers into 3 on the X and also the Y axis you have a calibrated “error corrected” preset that can capture your specimens in a way that it has every part 3 times captured on the X axis and 3 times on the Y axis.

During the process of modding the microscope to give it a digital scanning stage, I came along some other “problems” that I wanted to fix.

First of all since its such a big and strong heavy duty microscope its hard to travel with it and some parts can easily be replaced such as the second “side camera port” for something that is 3D printed out of ABS. The “side camera port” is about 400–450 grams and is not used and because of the hole it always is more vulnerable for dust. So It was time to combine this with the micro controller box that along the way found its place in the side port. Not only saving weight (300 -350 grams) but also preventing dust of getting in and having in the same time a nice place to have the electronics to control the digital scanning stage.

Next to that the specimen stage plate and clip were old and worn so this could also use an upgrade so it would become a two in one stage plate with specimen clip together + it would also be able to rotate free.

Another problem was the worn out socket for the lamp in the “illumination post” every time the cord was in the socket it was wobbling everywhere and it was not properly hold by the socket any more. So also this needed a good fix.

But lets start with the digital scanning stage additions before I show you the other small modifications.


General note: all parts are custom designed by me in Autodesk fusion 360 and printed on my Ultimaker2+ 3D printer with black ABS Ultimaker filament. Most of the parts are printed at 0.2 layer hight with 25 to 100% infill with a 0.4mm nozzle using the Cura slicer.

Other parts that are used next to the 3D printed parts will be described in detail below.

Below you can find more information on the parts that are added to the microscope including the parts for the Digital photography scanning stage.

The Control board & enclosure:
Along the way I figured out that this would be the prefect spot to put al the electronics needed for the controls of the step motors and camera. Below you see the two 3d render previews the enclosure. The enclosure should hold the Makeblock Orion control board, 2 step motor drivers and a Me shutter units to control the step drivers and camera trough the software.

Autodesk Fusion 360 — Bottom  Render of the “Controller enclosing”

Autodesk Fusion 360 — Top  Render of the “Controller enclosing”

“Controller enclosing” placed in the old second camera viewing port.

Item list: 
- The 2–3D printed parts
- 4 x M4 bolts (come with the second viewing port of microscope) 
- 4 x M3 bolts 10mm
- 6 x m4 bolts 6mm
- 1 x Makeblock orion main board 
- 2 x Step motor driver of Makeblock
- 1 x Me shutter Makeblock
- 1 x micro usb cable
- 1 x 12v 2A power adapter
- 2 x 10mm shrink wrap sleeves of 1 meter
- 3 x RJ-45 jack cables

Step motor bracket for X axis:
To control the X axis of the stage, I needed to create a clamp that would hold the step motor (otherwise it would turn itself instead of the shaft) to directly drive the old knob used to control the X axis manually. By removing the knob I was able to connect the drive shaft to the step motor with a Shaft Coupling Coupler. Doing this would result in turning the inner drive shaft in the the tube of the X and Y controls.

Autodesk Fusion 360 — Render of the “step motor connector for the X stage control”

“Step motor connected to the x stage knob”

Item list: 
- The 3–3D printed parts
- 4 x M3 bolts (come with the step motor) 
- 4 x M4 bolts 6mm
- 2 x M3 bolts 10mm
- 2 x M3 nuts hexa
- 1 x step motor 
- 1 x Shaft Coupling Coupler

Step motor bracket for Y axis:
Just like the X axis the Y axis also needed to be controlled. Only this was a bit harder since it would become quite hard for me to control both X and Y from the same “handle”. Since the “handle” which controls both X and Y has a inner and outer shaft / axis controlled by a knob to drive the table.

So I choose not to use the standard gear / knobs used in manual control for the Y axis. To solve this I added the step motor to a fixed part of the table that would move along in a fixed position with the Y or X axis. By doing this I was able to “push and pull” the table with a time belt along its Y axis feely, no matter where the table would move to.

Basically the bracket of step motor and pulley were attached to the part of the stage that was fixed. Driving the time belt to the made part of the table called the Gear Pulley Bracket that will be explained further bellow. Between this bracket of the Y axis step motor and the Gear Pulley Bracket the time belt would be a connection to the moving part of the Y table, “pushing or pulling” the table along the time belt connector.

I hope this explanation is clear enough, since it’s quite complicated sometimes to explain in words how it works, so please scroll down to see some of the images attached that hopefully make the principle more clear.

Autodesk Fusion 360 — Render of the “step motor connector for the Y stage control”

Step motor connected to stage table and the time belt with gear.

Item list: 
- The 3D printed part
- 4 x M3 bolts (come with the step motor) 
- 3 x M3 bolts 10mm
- 1 x step motor
- 1 x MXL Timing Belt
- 1 x Pulley 18T MXL

Stage time belt connector:
To move the stage I needed to connect the time belt to the Y moving part of the stage. Therefore I removed some of the original parts and placed a time belt connecter under the stage that would then squeeze in the time belt between a “clamping Mechanism”. With this clamp the time belt movement would be directly moving the stage when the time belt is being moved into small steps by the Y step motor.

Autodesk Fusion 360 — Render of the “Stage time belt connector”

Stage time belt connector connected to the stage and time belt.

Item list: 
- The 2 3D printed parts
- 2 x M2 bolts (Phillips screw) 6mm length
- 2 x M4 bolts (the 2 originals of the microscope stage) 
- 1 x time belt joiner

Gear Pulley Bracket:
To control the Y axis it was necessary to get a “gear pulley bracket on the end of the microscope stage to keep the timing belt running from the Y axis stepper motor, to to this I needed to connect it right after the macro and micro knob that normally controls the microscope stage manually. The extension beyond the table was necessary, to be able to get the full movement of the table.

Autodesk Fusion 360 — Render of the “Gear Pulley Bracket”

Images of the current situation and attachment to the table.

Item list: 
- The 3D printed part
- 2 x M3 bolts (original from stage assembly) 
- 1 x 50mm long axis of 4mm ų
- 1 x Pulley 18T MXL Timing Belt

Stage plate and specimen clip :
The microscope “originally” came with no specimen clip that would fit nicely with it, and I always struggled with the one I had. The one that I had did not work cause the stage plate that came with the microscope was a few mm to high and the connection points for the screws did not match the holes in the stage. Resulting in some weird problems such as not keeping the slides nicely in place. Also the clearance of objectives did not always go without problems since if to long they would hit the plate at the bottom if it was not centred right in the middle of the stage plate opening. So it needed to be bigger not a 20mmm diameter opening but more like 60mm large diameter opening.

So this means the stage plate should be re designed in a way it would be exactly as high as the top of the stage, it should hold the glass slides without the use of an extra specimen clip, have more clearance for the objectives to switch in the revolver, plus it would be a big advantage if the plate with the specimen could turn 360 degrees. These ideas and specs resulted in the following stage plate.

The only thing that I will do in the next update, is to make the extruded lowered part for the glass slide with less tolerance so it will fit in exact so there is no chance of moving during the scanning process.

Autodesk Fusion 360 — Render of the “stage plate with specimen slide holder”

Stage specimen plate clip in place.

Lamp socket fix:
Since the lamp socket was quit heavily used in the last 30+ years and quite worn out, I wanted to create a socket where you can put the power plug in without the plug moving or hanging weirdly resulting in failure over time. The design and solution I came to was as follow.

Autodesk Fusion 360 — Render of the “Lamp socket fix”

Lamp cable into stable socket connector.

Item list: 
- The 3D printed part
- 1 x M3 bolt 25mm

Below you will see four images that will give you a “360” view of the final result of the microscope.

Complete “360” view on the final result of the modded microscope.

I’m very happy about this result and the current “final” state its in. But knowing my self, I already have some new ideas on the addition of hardware and software, but more about this can be found below.

For now it’s time to show you the “power” of the microscope and its scanning table software and hardware. Below you will find a short movie that shows the hardware moving controlled by the custom made software on the laptop that stands next to it.

Some of the hardware movements controlled by the software. Some part are with big steps 150–300 steps at a time and others are 1 to 25 steps at a time making it way more accurate. The smallest step possible to make is 0.01mm measured with a calibrated um microscope ruller.

To make it “simple”, there are two parts that make the scanning stage work like it does now.

1.) Main board:
The main board and the connected hardware; this main board is programmed with several functions (I will go into more detail about this later) with the use of the Arduino IDE programmer. The code language used in this platform is C/C++. This board is then connected trough usb with the laptop.

2.) Software:
There is a code running on the laptop that communicates with the main bord trough a serial port over usb. This code is written in the Processing IDE (that uses JAVA). Because the main board is programmed to run several functions, we now only have to say in the software which function we want to run and how we want to run it (declare the values of the variables). To make this easy we use a GUI that displays the functions and the variables that can be set. Once these are set and “uploaded” you can control the microscope with the settings used.

A screenshot of the GUI that communicates with the control board trough the serial port

Above you see a screen shot of the GUI. I tried to keep this piece of software and GUI as simple as I could, but in the future I hope to tweak and update it and give more functions (more about this later).

The first step when the software is opened is to select the lens you are going to use. The larger the enlargement of the objective the smaller calibrated steps it wil take. The size of the steps are visible after selecting the lens, in the box STEP SIZE X or STEP SIZE Y. Accordingly you can also manually change them if they don’t suit your way of examining your specimen.

When you are examining your specimens or when you want to “guide” the table to a specific location you can simply use your keyboards arrow keys. the way you would normally do to navigate trough for example a game. Left is left and right, up and down are mapped down in the same way you would normally expect. You can ether press the keys once to have 1 accurate step or hold it for continues movement.

After you have examined your specimen and choose the part you want to image find your start location.

When choosing your start location t is important to pick a spot that is say a 3 frames on the X and Y axis away from the top left corner of the area you want to index.

Once you have chosen your start location (top left) you have to “guess” the amount of frames you think you would need to index the specimen at the enlargement you are using. If you know you need +/10 frames on the X and 10 on the Y you can fill this into the boxes under “GRID SIZE CONTROLS” and set it to FRAMES X: 10 and FRAMES Y: 10. After this you can press apply and the software wil “upload” the data to the board.

To be sure the area that you want to capture is fully in the frame you can press the TEST SEQUENCE button. In this case it wil start a quick movement of 10 frames down -> 10 frames to the right -> 10 frames up -> 10 frames to the left. In other words it will “draw” a outline around your specimen area. When you watched thought the oculars, or payed attention to the screen you find out if the area was to small or to big. If to big or to small you can change the values accordingly. Once you found the correct grid size you can re apply you settings and press the START button. Now the software will start to capture the amount of frames set in the X and Y boxes.

Reading the above might not give you a full idea of how this then works when used, so I made a screen recording while I’m using the scanning stage. Below in the video you see the proces of photographing a crystallized tear with an total enlargement of 250X (10X objective 10X oculair 2.5X Camera), resulting in the final result of a 300 MP ( 17364 x 17364 pixels) photo of a crystalized tear.

Video showing a screen recording of the software in use and the progress during the capturing of the images when the DIY scanning stage is in use. This is a accelerated version of the +/- 25–35minute process. ( The images are taken with a 10x objective resulting with the camera in a total enlargement of 250X).

The scanning / capturing time of this image was +/- 25 minutes for the , resulting in 350 images shot in RAW format captured with my Canon 5D MKIIII. With a total movement of 2,7MM in the X and Y direction (+/-150um per step).

*Time of 25 minutes can be reduced since the time is now standard set to wait for 1,5 second before taking an image, to stabilise the table after movement. Then giving the camera time to do and exposure up to 1 second, and then 1 second to do the next movement. So in total every step / frame will take 4 seconds making it a total time of 4x 250 =23,3 minutes.

During the capturing the images are automatically downloaded to a folder cropped and saved as a .TIFF. So directly after all the images are shot you can start your post process of stitching and rendering your images together with your favorite stitching / panorama software (in my case Autopano Giga ) which then takes around 30–40 minutes for a images of this size to complete (loading, pre- render, render and export).

Screenshot of the 350 images pre-rendered by Autopano Giga, showing a great RMS score.

Subtotal time: Time spent on creating a 300MP image without other photoshop processing is about +/- 60 minutes.

After this render its often needed to spend some time to create the finalised crystalised tear image since I want them to be perfect. Depending on the stitching quality and small errors this takes about 30–60 minutes. You can find the final image below, or by following this link to see it in 300+ MP.


Total time: spent on creating a 300MP image with minor corrections, fixes, color corrections, level adjustments and background replacement in photoshop is about +/- 80 minutes.

Software summery:

1.) EOS utility
- Directly controlling the camera
- Directly downloading the images from the camera connected trough USB.
- Live view to during the process to see what its doing.

*While the EOS software is directly downloading the images through the tethering usb connection a program in the background scans the folder and converts the images to .TIFF and crops them into 1:1 aspect ratio and saves them in a _cropped_ folder. The coping is done to eliminate the vignetting and unsharp characteristics of the objectives in the microscope.

2.) Autopano Giga
- To load in the images that were directly downloaded to a folder on the computer with EOS utility.
- Index, process and render out the stitched file created from the images imported.

3.) Photoshop CS
- To finalise the rendered image of Autopano Giga by checking and removing / editing the image so it can be finalised.

Since my mind often is full of new ideas when I’m not even ready with the frist version I decided this time to first present you this version and later extent its features software and hardware wise. So what will I be adding in the future?

Direct input towards the main board making it able to stand alone working without a laptop.

1.) Adding a touch screen display so I don’t need to use the GUI and software on laptop.
2.) Adding a joystick to smoothly control the movements instead of using laptops keyboard
3.) Adding a Accelerometer that is checking for vibrations. If there would be a spike, due a bump against the table where the microscope is standing on it will stop and roll back and re take previous image.
4.) Adding a endstop switch so the software knows its 0 position.
5.) SD card for logging the steps so it always knows what it did and can roll back accordingly.
6.) Finetuning the time belt and gear settings to be even more accurate
7.) Adding a Kinect camera or other like camera to track objects and movements under the microscope.
8.) Z axis step motor

Some of the hardware options above require new software or software additions to make it work.

1.) Rewriting the software for the main board so it can also be used in stand alone mode
2.) Adding joystick support
3.) Adding error handeling support for the Accelerometer when triggered
4.) Adding end stop switch 0 position and “re calibration” of the scanning stage before it starts. And when the progress is done return back home, or to its starting position.
5.) Read out log plot positions
6.) More step motor control options that make several ways of moving possible:
6b.) tracking an object that is viewed with the 2nd camera (Kinect) and keeping it centred.
6c.) Smoother transitions due ease- in and out functions.
6d.) Drawing shapes that are converted into movements of the table so if you film a slide you can set dynamic shapes and patterns with according ease functions.
7.) Start / stop / pause button
8.) Elapsed time, shutter count and % progress
9.) Control of the Z axis so the images can also be stacked.
10.) Camera exposure time
11.) Waiting time between images.

So there is still some development going on and I would love to give you some more updates soon.

If you have any questions, suggestions or feedback regarding this article, then please feel free to contact me.