Abstract

In recent years, the development of smart drug delivery systems based on biodegradable polymeric nanoparticles has become of great interest. Drug-loaded nanoparticles can be introduced into the cell interior via endocytotic processes followed by the slow release of the drug due to degradation of the nanoparticle. In this work, poly(L-lactic acid) (PLLA) was chosen as the biodegradable polymer. Although common degradation of PLLA has been studied in various biological environments, intracellular degradation processes have been examined only to a very limited extent. PLLA nanoparticles with an average diameter of approximately 120 nm were decorated with magnetite nanocrystals and introduced into mesenchymal stem cells (MSCs). The release of the magnetite particles from the surface of the PLLA nanoparticles during the intracellular residence was monitored by transmission electron microscopy (TEM) over a period of 14 days. It was demonstrated by the release of the magnetite nanocrystals from the PLLA surface that the PLLA nanoparticles do in fact undergo degradation within the cell. Furthermore, even after 14 days of residence, the PLLA nanoparticles were found in the MSCs. Additionally, the ultrastructural TEM examinations yield insight into the long term intercellular fate of these nanoparticles. From the statistical analysis of ultrastructural details (e.g., number of detached magnetite crystals, and the number of nanoparticles in one endosome), we demonstrate the importance of TEM studies for such applications in addition to fluorescence studies (flow cytometry and confocal laser scanning microscopy).

Highlights

  • Nowadays biocompatible and biodegradable polymers are customary materials in daily medical routine

  • In order to cope with these problems we used tailor-made, poly(L-lactic acid) (PLLA) nanoparticles containing a fluorescent marker (PMI) suitable for flow cytometry and laser scanning microscopy (LSM) measurements

  • Our results demonstrate that after uptake into mesenchymal stem cells (MSCs), the PLLA nanoparticles undergo intracellular degradation

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Summary

Introduction

Nowadays biocompatible and biodegradable polymers are customary materials in daily medical routine. By tailoring their macromolecular architecture, it is possible to precisely adjust mechanical properties as well as features for interaction with living organisms, for example, the decomposition dynamics of resorbable threads in surgery or the surface compatibility of bone implants. The decomposition of poly(L-lactic acid) (PLLA) takes place via hydrolysis when exposed to an aqueous environment and can be enzymatically catalyzed [2]. The decomposition of macroscopic PLLA implants has already been shown in vitro and in vivo [5,6,7,8] and can be accelerated by the presence of enzymes or bacteria. It is speculated that L-lactic acid, which is the degradation product of PLLA, is transformed into water and CO2 via the citric acid cycle [9]

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