Kinetics and the Theoretical Aspects of Drug Release from PLA/HAp Thin Films

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.The theory of dissolution kinetics of gentamicin from polylactic acid-hydroxyapatite thin film composites is spotlighted with the combination of diffusion and polymer degradation modeling. The use of various mathematical models, characterizing diffusion, dissolution or/and erosion prevalence as well as a mix of dissolution-diffusion rate processes were employed in order to compare theory with experimental data. A number of factors influence the release kinetics of gentamicin from medical drug release systems and devices. It is difficult to have a single mathematical model that takes all these factors into account. It is shown that the degradation of the polymer matrix plays the biggest role in the release kinetics of polymer-ceramics thin film composites. It was also observed that multistage drug release form these devices depends also on the degradation kinetics of the polymer matrix. The effect of pH and device sizes were not studied but could also be of interest in future studies

Drug Delivery From Polymer-Based Nanopharmaceuticals—An Experimental Study Complemented by Simulations of Selected Diffusion Processes

The success of medical therapy depends on the correct amount and the appropriate delivery of the required drugs for treatment. By using biodegradable polymers a drug delivery over a time span of weeks or even months is made possible. This opens up a variety of strategies for better medication. The drug is embedded in a biodegradable polymer (the “carrier”) and injected in a particular position of the human body. As a consequence of the interplay between the diffusion process and the degrading polymer the drug is released in a controlled manner. In this work we study the controlled release of medication experimentally by measuring the delivered amount of drug within a cylindrical shell over a long time interval into the body fluid. Moreover, a simple continuum model of the Fickean type is initially proposed and solved in closed-form. It is used for simulating some of the observed release processes for this type of carrier and takes the geometry of the drug container explicitly into account. By comparing the measurement data and the model predictions diffusion coefficients are obtained. It turns out that within this simple model the coefficients change over time. This contradicts the idea that diffusion coefficients are constants independent of the considered geometry. The model is therefore extended by taking an additional absorption term into account leading to a concentration dependent diffusion coefficient. This could now be used for further predictions of drug release in carriers of different shape. For a better understanding of the complex diffusion and degradation phenomena the underlying physics is discussed in detail and even more sophisticated models involving different degradation and mass transport phenomena are proposed for future work and study

Comparative study of coral conversion, Part 3: Intermediate products in the first half an hour

International audienceDifferent methods to produce calcium phosphate materials have been well established and are currently used by both scientific and industrial community. While other new and more economical production techniques are under development, the actual reactions mechanisms involve in these techniques are not well understood. Understanding what really happen during reaction will pave a way to tune the final product for well-defined morphology and purity. We focused into improving in-depth understanding of the reaction mechanisms and the intermediates products participating in the reaction of coralline materials with orthophosphoric and ammonium phosphate solutions under mechano-chemical reaction technique. The results suggest that within 30 minutes of reaction under ammonium phosphate solution only HAp phase is produced through solid-state iron exchange reaction. On the other hand, under orthophosphoric acid solution, intermediate phases such as octacalcium phosphate (OCP) and monetite form and convert to hydroxyapatite HAp at different times. Other phase that formed as an intermediate was identified as brushite. It was also observed that pH plays a big role in the formation of these phases due to their different pH stability. The results also confirm our previous hypothesis that under orthophosphoric acid phosphate solution the reaction mechanism is dissolution-recrystallization while under ammonium phosphate solution is solid-state topotactic ion exchange reaction mechanism. It is envisaged that there are possibilities of the formation of intermediate products within or before the first 5 minutes of reaction

Comparative study of Coral Conversion, Part 2: Microstructural evolution of calcium phosphate

International audienceCalcium phosphate materials can be easily produced by a number of wet chemical methods that involve both acidic and basic environments. In our previous study, we investigated calcium phosphates such as monetite, hydroxypatite and whitlockite which were successfully produced by mechano-chemical method from corals obtained from the Great Barrier Reef. It was observed that a number of synthesis factors such as the pH of the environment, the reaction temperature and the chemistry influenced the crystal size formed. A number of theories have been suggested on the mechanisms of crystal formation; however, very few mechanisms have been universally accepted. The present work was aimed to explore the evolution of crystalline calcium phosphate and their morphology with respect to the pH of the environment and reaction time. Conversion of coral to calcium phosphates was carried out with stoichiometric amount of required H3PO4 or (NH4)2HPO4, to obtain hydroxyapatite (HAp) or tri calcium phosphate (TCP) phases. The acidic or basic solution was added, drop wise, at a rate of 2 mL min-1, to 6 g of coral powder suspended in 300 mL of distilled water at 80 ± 0.5°C on a hot plate with magnetic stirrer. The pH of reaction was monitored. Crystal morphology and the phases were identified by XRD, FTIR, and SEM studies. It was observed that under acidic conditions (H3PO4), dissolution and then precipitation influences the crystal morphology and transition from plate like to rod like hydroxyapatite structure. During the first hour of the dissolution a monetite and hydroxyapatite mixture precipitates and then the full conversion to hydroxyapatite is observed. However under basic conditions (NH4)2HPO4), pH is only marginally changed within the environment and just surface conversion of the calcium carbonate structure of coral to hydroxyapatite and a very small amount of tri-calcium phosphate is observed. The mechanism can be classified as the solid state topotactic ion-exchange reaction mechanism