Team:Evry/Pill design

From 2013.igem.org

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<h1> Capsule design </h1>
<h1> Capsule design </h1>
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<div class="center"><i>a transport device to deliver our bacteria to the intestine</i></div>
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<div class="center"><i>a transport device to deliver <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b> to the intestine</i></div>
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To effectively treat iron over-absorption, our engineered bacteria need to be delivered to the distal area of the duodenum and the proximal area of the jejunum. We thus designed a capsule with a methacrylic acid exterior that resists the low pH conditions in the stomach, but will dissolve at intestinal pH. The capsule interior contains colloidal silica and hydroxypropylmethylcellulose (HPMC), which ensures that the bacteria survive in the capsule and have enough time to uptake iron when released in the intestine.<br>
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To effectively treat iron over-absorption, we needed a device to deliver our <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b> bacteria to the distal area of the duodenum and the proximal area of the jejunum. Additionally, we want to give <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b> <a href="https://2013.igem.org/Team:Evry/Model3">enough time to produce enterobactins</a>. We thus designed and built a capsule with a methacrylic acid exterior that resists the low pH conditions in the stomach, but will dissolve at intestinal pH to release <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b>. The capsule interior contains colloidal silica and hydroxypropylmethylcellulose (HPMC), which ensures that the bacteria survive in the capsule and have enough time to uptake iron when released in the intestine.<br>
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<img src="https://static.igem.org/mediawiki/2013/5/5f/Capsule_legende.png" alt="capsule_legend" width="40%"/>
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First, we create a <b>novel capsule following the <a href="https://2013.igem.org/Team:Evry/Pill_design#Norms" >actual norms</a> from the European Pharmacopeoa</b> concerning gastro-enteric resistant formulations.<br><br>
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First, we create a <b>novel capsule following the actual norms from the European Pharmacopeoa</b> concerning gastro-enteric resistant formulations.<br><br>
Second, we ensure that the bacteria survive following dissolution of the capsule.
Second, we ensure that the bacteria survive following dissolution of the capsule.
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We see three main challenges. First, <b>the capsule must resist the low pH conditions in the stomach</b>, which are lethal to our bacteria. Second, <b>the capsule must rapidly dissolve in the duodenum</b> to deliver its payload to the distal duodenum and the proximal jejunum. Third, <b>the bacteria must have enough time to effectively uptake iron</b>
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We see three main challenges to construction of a device to deliver bacteria to the intestine. First, <b>the capsule must resist the low pH conditions in the stomach</b>, which are lethal to our bacteria. Second, <b>the capsule must rapidly dissolve in the duodenum</b> to deliver its payload to the distal duodenum and the proximal jejunum. Third, <b>the bacteria must have enough time to produce enterobactins to effectively uptake iron</b> before being excreted from the intestine.
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The first step in the design of our pill is to determine its galenic formulation. We want a <i>per os</i> administration for our bacteria and had the choice between either a tablet or a capsule. A tablet requires a heavy and dry compression and the bacteria in a lyophilized form, entailling high temperatures and pressures that would result in significant bacterial mortality. We decided a a capsule is more suited for our purpose because it offers the possibility to contain a non-compressed powder and avoids a lyophilization step, thus representing a more favorable environment for bacteria storage. In addition, a capsule avoids lyophilizing the bacteria, which would delay their metabolic activity after being released.
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The first step is to determine the galenic formulation of our pill. We want a <i>per os</i> administration for our bacteria and had the choice between either a tablet or a capsule. A tablet requires dry compression of its contents, meaning the bacteria would have to be lyophilized. We decided a capsule is more suited for our purpose because it can contain a non-compressed powder and avoids lyophilization, which would result in a significant delay in metabolic activity of the bacteria after being released.
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A pharmaceutical capsule requires every component to be in powder form. We tested which formulation was able to absorb the most LB medium saturated with bacteria. In galenic research, this is called a <i>moisture absorbent</i> and ensures the proper chemical properties to keep our drug (here our bacteria in LB medium) viable in a dry environment. We experimented with several compositions based on <i<maltodextrin</i> and <i>colloidal silica</i> (figure 1 and 2). Our final choice was <i>colloidal silica</i>.</p>
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A pharmaceutical capsule requires every component to be in powder form. We tested which formulation was able to absorb the most LB medium saturated with bacteria. In galenic research, this is called a <i>moisture absorbent</i> and ensures the proper chemical properties to keep our drug (here our bacteria in LB medium) viable in a dry environment. We experimented with several compositions based on <i>maltodextrin</i> and <i>colloidal silica</i> (Figures 1 and 2) and found <i>colloidal silica</i> interacted better with LB medium.</p>
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For the next step, we want to increase the volume to 35 mL which is the sufficient amount to make 50 capsules (standard for one rack, figure 3). Thus, a <i>diluent</i> is required and we opted for HPMC (hydroxypropylmethylcellulose). The entire volume of powder has to be equally distributed in the capsules (figure 4).
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We produced capsules in batches of 50 (standard for one rack, Figure 3). Here we carefully mix colloidal silica with the HPMC <i>diluent</i> such that the entire volume of powder is equally distributed in the capsules (Figure 4).
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Finally, the 50 capsules contain all together 11 ml of colloidal silica (where 4 mL of saturated bacteria have been dissolved in) and 24 mL of HPMC. The last step is the closing of the capsules (figure 5 and 6).
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Finally, the 50 capsules contain a total of 11 ml of colloidal silica in which 4 mL of saturated bacteria have been dissolved in 24 mL of HPMC. The last step is sealing the capsules (Figures 5 and 6).
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<div align="center"><img src="https://static.igem.org/mediawiki/2013/3/33/IC_protected_against_acid.jpg" alt="Capsule" width="20%"/></div>
<div align="center"><img src="https://static.igem.org/mediawiki/2013/3/33/IC_protected_against_acid.jpg" alt="Capsule" width="20%"/></div>
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<h3>How to overcome the acidity of the stomach?</h3>
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<h3 id="acidity">How to overcome the acidity of the stomach?</h3>
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It is very common in pharmaceutical galenical research to overcome the acidity of the stomach and to target the duodenum/jejunum for medical delivery. To this end, we soaked the capsule in an ethanol-based solution of methacrylic acid and dried it with hot air. This method produced a capsule with a double envelope that resists gastric acidity.  
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It is a common challenge in pharmaceutical galenical research to bypass the acidity of the stomach and target a medicine to the duodenum/jejunum. To this end, we soaked the capsule in an ethanol-based solution of methacrylic acid and dried it with hot air. This method produced a capsule with a double envelope that resists gastric acidity.  
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<h3>How to deliver the bacteria in the jejunum?</h3>
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<h3 id="jejunum">How to deliver the bacteria in the intestine?</h3>
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The delivery in the duodenum/jejunum is already possible due to the gelatine-based composition of the capsule. In contact to water, the capsule dissolves and delivers its containment in the duodenum. This is only feasable when the capsule has already resisted to the gastric acidity. Moreover, we added a HPMC as a diulent. In the presence of water, right after the dissolution of the gelatine capsule, it is able to swell. Depending on its density, the polymere forms a more or less viscuous obstruction. This process creates an environment in the jejunum where bacteria can statically proliferate. Thus, HPMC, beside its properties as a <i>diluent</i>, is also called a <i>bio-adhesive</i> for its ability to stick to the membranes of the intestins and form an obstruction.
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The gelatine-based composition of the capsule dissolves at neutral pH to deliver its payload to the duodenum. Right after the dissolution of the gelatine capsule, the HPMC swells to form a viscuous obstruction. This process creates an environment in the jejunum where bacteria can statically proliferate. Thus, HPMC, beside its properties as a <i>diluent</i>, is also called a <i>bio-adhesive</i> for its ability to stick to the membranes of the intestins and form an obstruction.
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     <b>Figure 10:</b> The basket that dips into the solution.
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     <b>Figure 10:</b> Basket that dips the capsules into a liquid solution.
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The dissolution machine is able to lift a basket up and down into a 800mL beaker (figure 9). For every experience, we were able to test 6 capsules spread into 6 apart columns (figure 10). Keep in mind that these columns have the possibility to be closed by a lid on the top to increase the dissolution and mimic different segments of the intestins.
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The dissolution machine lifts raises and lowers a basket into a 800mL beaker (Figure 9). In each experiment, we were able to test 6 capsules spread into 6 separate columns (Figure 10). These columns can be sealed on top with a lid to increase the dissolution and mimic different segments of the intestines.
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     <b>Figure 11:</b> Capsule dissolvement stage after 1 hour of exposure to gastric acid.
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     <b>Figure 11:</b> The capsules do not dissolve after 1 hour of exposure to gastric acid.
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     <b>Figure 12:</b> Water turbidity after 1 hour of exposure to gastric acid.
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     <b>Figure 12:</b> The acid solution is clear after containing the capsules for 1 hour.
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We observe that after one hour of exposure to gastric acidity, the capsules are not dissolved. They kept their integrity (figure 11) and didn't deliver its contanment (figure 12).
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We observed that the capsules maintained their integrity after one hour of exposure to gastric acidity (Figure 11) and didn't release their contents into solution (Figure 12).
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     <b>Figure 13:</b> Capsule dissolvement stage after 2 hours of exposure to gastric acid.
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     <b>Figure 13:</b> Capsules resist dissolving after 2 hours of exposure to gastric acid.
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     <b>Figure 14:</b> Water turbidity after 2 hours of exposure to gastric acid.
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     <b>Figure 14:</b> The acid solution remains clear after containing the capsules for 2 hours.
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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We continued the experiment for an additional hour to confirm that even after two hours of exposure to a pH=2 solutes, the capsules were still not dissolved (Figure 13) and hadn't released their contents (Figure 14).
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     <b>Figure 15:</b> Final solution color after 2 hours of exposure to gastric acidity.
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     <b>Figure 15:</b> Final acid solution color after containing the capsules for 2 hours.
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We observe that the water is very clear (figure 15), thus meaning that the first condition of the European Pharmacopeoa to create a gastro-enteric resistant capsule is fullfilled.
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The acid solution was clear after removing the capsules (Figure 15), showing that the first condition of the European Pharmacopeoa to create a gastro-enteric resistant capsule has been fullfilled.
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     <b>Figure 17:</b> Water turbidity after 0 minute of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 17:</b> PBS (pH = 7,2) turbidity at the beginning of the experiment.
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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The capsules were fully intact when they were transferred to a PBS (Figure 16) and none of the contents were immediately released (Figure 17).
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     <b>Figure 18:</b> Capsule dissolvement stage after 15 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 18:</b> Capsules begin dissolving after 15 minutes in PBS buffer (pH = 7,2).
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     <b>Figure 19:</b> Water turbidity after 15 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 19:</b> PBS buffer turbidity after containing capsules for 15 minutes.
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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The capsules began to dissolve after 15 minutes in PBS buffer (Figure 18) and the dye solution began to be released (Figure 19).
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     <b>Figure 20:</b> Capsule dissolvement stage after 30 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 20:</b> Capsules after 30 minutes in PBS.
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     <b>Figure 21:</b> Water turbidity after 30 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 21:</b> PBS turbidity after containing capsules for 30 minutes.
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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The capsules continue to dissolve after 30 minutes in PBS buffer (Figure 20) and released their contents (Figure 21).
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     <b>Figure 22:</b> Capsule dissolvement stage after 40 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 22:</b> Capsules after 40 minutes exposure to PBS buffer (pH = 7,2).
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     <b>Figure 23:</b> Water turbidity after 40 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 23:</b> PBS turbidity after containing capsules for 40 minutes.
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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The capsules continue to dissolve after 40 minutes in PBS buffer (Figure 22) and release their contents (Figure 23).
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     <b>Figure 16:</b> Capsule dissolvement stage after 50 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 24:</b> Capsule dissolution after 50 minutes in PBS buffer (pH = 7,2).
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     <b>Figure 17:</b> Water turbidity after 50 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 25:</b> PBS turbidity after containing capsules for 50 minutes.
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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The capsules continue to dissolve after 50 minutes in PBS buffer (Figure 24) and release their contents (Figure 25).
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     <b>Figure 16:</b> Capsule dissolvement stage after 60 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 26:</b> Capsules were fully dissolved after 60 minutes in PBS buffer (pH = 7,2).
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     <b>Figure 17:</b> Water turbidity after 60 minutes of exposure to PBS buffer (pH = 7,2).
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     <b>Figure 27:</b> The PBS turbidity after 60 minutes of exposure to PBS buffer (pH = 7,2).
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We observe that after two hours of exposure to gastric acidity, the capsule are still not dissolved. They kept their integrity (figure 13) and didn't deliver its contanment (figure 14).
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The capsules were fully dissolved after 60 minutes in PBS (Figure 26) and had released their contents into the PBS solution (Figure 27).
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<h2 id="conclusion">Conclusion and perspectives</h2>
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Our polymeric capsule successfully bypassed stomach acidity (pH=2) and rapidly dissolved to release its contents at neutral pH as in the duodenum and jejunum. The capsule thus fulfills the requirements of the European Pharmacopeia.
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The purpose of this capsule is to <a href="https://2013.igem.org/Team:Evry/Model3>slow down the flush of bacteria</a> right after it is delivered in the duodenal region. Bacteria don't have enough time to produce their iron chelators. The addition of HPMC will create an obstruction in the area of iron absorption to allow enterobactin production.
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Also, we calculated its cost and evaluated the <a href="https://2013.igem.org/Team:Evry/Economy"> impact</a> such a treatment could have on the health system. Blood-lettings are expensive and this treatment can be seen as an alternative or a complement to blood-lettings.
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The next step for the capsule project is to mix the colloidal silica and hydroxypropylmethylcellulose with a concentrated culture of our siderophore-overexpressing <b><span style="color:#bb8900">Iron</span><span style="color:#7B0000"> Coli</span></b>. After encapsulating them in gelatine and methacrylic acid, we must establish that our bacteria can be released from the capsule and survive. If these tests are conclusive it could be possible to test the capsule in hemochromatosis mice.
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Latest revision as of 03:07, 29 October 2013

Iron coli project

Capsule design

a transport device to deliver Iron Coli to the intestine



Bannière gélule

Abstract

To effectively treat iron over-absorption, we needed a device to deliver our Iron Coli bacteria to the distal area of the duodenum and the proximal area of the jejunum. Additionally, we want to give Iron Coli enough time to produce enterobactins. We thus designed and built a capsule with a methacrylic acid exterior that resists the low pH conditions in the stomach, but will dissolve at intestinal pH to release Iron Coli. The capsule interior contains colloidal silica and hydroxypropylmethylcellulose (HPMC), which ensures that the bacteria survive in the capsule and have enough time to uptake iron when released in the intestine.

capsule_legend

First, we create a novel capsule following the actual norms from the European Pharmacopeoa concerning gastro-enteric resistant formulations.

Second, we ensure that the bacteria survive following dissolution of the capsule.


Capsule design requirements

We see three main challenges to construction of a device to deliver bacteria to the intestine. First, the capsule must resist the low pH conditions in the stomach, which are lethal to our bacteria. Second, the capsule must rapidly dissolve in the duodenum to deliver its payload to the distal duodenum and the proximal jejunum. Third, the bacteria must have enough time to produce enterobactins to effectively uptake iron before being excreted from the intestine.

Capsule design, step by step


Capsule

Which galenic formulation is best suited for our goals?

The first step is to determine the galenic formulation of our pill. We want a per os administration for our bacteria and had the choice between either a tablet or a capsule. A tablet requires dry compression of its contents, meaning the bacteria would have to be lyophilized. We decided a capsule is more suited for our purpose because it can contain a non-compressed powder and avoids lyophilization, which would result in a significant delay in metabolic activity of the bacteria after being released.


Capsule

How to store the bacteria in the capsule?

Iron minion
Figure 1: Testing both moisture absorbents.
Iron minion
Figure 2: Hand mortar and pestle, old fashioned but efficient.

A pharmaceutical capsule requires every component to be in powder form. We tested which formulation was able to absorb the most LB medium saturated with bacteria. In galenic research, this is called a moisture absorbent and ensures the proper chemical properties to keep our drug (here our bacteria in LB medium) viable in a dry environment. We experimented with several compositions based on maltodextrin and colloidal silica (Figures 1 and 2) and found colloidal silica interacted better with LB medium.



Iron minion
Figure 3: Preparing the rack with 50 empty capsules.
Iron minion
Figure 4: Filling the capsule with the total amount of powder.

We produced capsules in batches of 50 (standard for one rack, Figure 3). Here we carefully mix colloidal silica with the HPMC diluent such that the entire volume of powder is equally distributed in the capsules (Figure 4).



Iron minion
Figure 5: Closing the capsules after a filling the rack.
Iron minion
Figure 6: Final result, 50 capsules uniformally filled with the powder mixture.

Finally, the 50 capsules contain a total of 11 ml of colloidal silica in which 4 mL of saturated bacteria have been dissolved in 24 mL of HPMC. The last step is sealing the capsules (Figures 5 and 6).



Capsule

How to overcome the acidity of the stomach?

Dipping
Figure 7: Dipping of the capsule in an alcohol-based methacrylic acid polymer solution.
Hairdryer
Figure 8: Drying of the capsule by evaporating the alcohol.


Capsule

How to deliver the bacteria in the intestine?

The gelatine-based composition of the capsule dissolves at neutral pH to deliver its payload to the duodenum. Right after the dissolution of the gelatine capsule, the HPMC swells to form a viscuous obstruction. This process creates an environment in the jejunum where bacteria can statically proliferate. Thus, HPMC, beside its properties as a diluent, is also called a bio-adhesive for its ability to stick to the membranes of the intestins and form an obstruction.


Capsule

How to prove the real efficiency of our capsule?

As a proof of concept, we fulfilled the two basic requirements of the European Pharmacopeia to make a gastro-enteric resistant capsule which are as follows:

  1. No dissolution of the capsule after 2 hours of exposure to gastric acid (solution at pH = 2)
  2. Dissolution of the capsule within 1 hour of exposure to water (Phosphate Buffer solution, pH = 7) right afterwards

Hairdryer
Figure 9: The dissolution machine.
Hairdryer
Figure 10: Basket that dips the capsules into a liquid solution.

The dissolution machine lifts raises and lowers a basket into a 800mL beaker (Figure 9). In each experiment, we were able to test 6 capsules spread into 6 separate columns (Figure 10). These columns can be sealed on top with a lid to increase the dissolution and mimic different segments of the intestines.




Capsule integrity 1 hour
Figure 11: The capsules do not dissolve after 1 hour of exposure to gastric acid.
Turbidity 1 hour
Figure 12: The acid solution is clear after containing the capsules for 1 hour.

We observed that the capsules maintained their integrity after one hour of exposure to gastric acidity (Figure 11) and didn't release their contents into solution (Figure 12).

Capsule integrity 2 hours
Figure 13: Capsules resist dissolving after 2 hours of exposure to gastric acid.
Turbidity 2 hours
Figure 14: The acid solution remains clear after containing the capsules for 2 hours.

We continued the experiment for an additional hour to confirm that even after two hours of exposure to a pH=2 solutes, the capsules were still not dissolved (Figure 13) and hadn't released their contents (Figure 14).

Final solution color
Figure 15: Final acid solution color after containing the capsules for 2 hours.

The acid solution was clear after removing the capsules (Figure 15), showing that the first condition of the European Pharmacopeoa to create a gastro-enteric resistant capsule has been fullfilled.




Capsule integrity 0 minute
Figure 16: Capsule dissolvement stage after 0 minute of exposure to PBS buffer (pH = 7,2).
Turbidity integrity 0 minute
Figure 17: PBS (pH = 7,2) turbidity at the beginning of the experiment.

The capsules were fully intact when they were transferred to a PBS (Figure 16) and none of the contents were immediately released (Figure 17).

Capsule integrity 15 minutes
Figure 18: Capsules begin dissolving after 15 minutes in PBS buffer (pH = 7,2).
Turbidity integrity 15 minutes
Figure 19: PBS buffer turbidity after containing capsules for 15 minutes.

The capsules began to dissolve after 15 minutes in PBS buffer (Figure 18) and the dye solution began to be released (Figure 19).

Capsule integrity 30 minutes
Figure 20: Capsules after 30 minutes in PBS.
Turbidity integrity 30 minutes
Figure 21: PBS turbidity after containing capsules for 30 minutes.

The capsules continue to dissolve after 30 minutes in PBS buffer (Figure 20) and released their contents (Figure 21).

Capsule integrity 40 minutes
Figure 22: Capsules after 40 minutes exposure to PBS buffer (pH = 7,2).
Turbidity integrity 40 minutes
Figure 23: PBS turbidity after containing capsules for 40 minutes.

The capsules continue to dissolve after 40 minutes in PBS buffer (Figure 22) and release their contents (Figure 23).

Capsule integrity 50 minutes
Figure 24: Capsule dissolution after 50 minutes in PBS buffer (pH = 7,2).
Turbidity integrity 50 minutes
Figure 25: PBS turbidity after containing capsules for 50 minutes.

The capsules continue to dissolve after 50 minutes in PBS buffer (Figure 24) and release their contents (Figure 25).

Capsule integrity 60 minutes
Figure 26: Capsules were fully dissolved after 60 minutes in PBS buffer (pH = 7,2).
Turbidity integrity 60 minutes
Figure 27: The PBS turbidity after 60 minutes of exposure to PBS buffer (pH = 7,2).

The capsules were fully dissolved after 60 minutes in PBS (Figure 26) and had released their contents into the PBS solution (Figure 27).


Conclusion and perspectives

Our polymeric capsule successfully bypassed stomach acidity (pH=2) and rapidly dissolved to release its contents at neutral pH as in the duodenum and jejunum. The capsule thus fulfills the requirements of the European Pharmacopeia.

The purpose of this capsule is to impact such a treatment could have on the health system. Blood-lettings are expensive and this treatment can be seen as an alternative or a complement to blood-lettings.

The next step for the capsule project is to mix the colloidal silica and hydroxypropylmethylcellulose with a concentrated culture of our siderophore-overexpressing Iron Coli. After encapsulating them in gelatine and methacrylic acid, we must establish that our bacteria can be released from the capsule and survive. If these tests are conclusive it could be possible to test the capsule in hemochromatosis mice.