Abstract

For the development of effective drug carriers, nanocapsules that respond to micro-environmental changes including a decrease in pH and a reductive environment were prepared by the stabilization of polymer vesicles formed from head-tail type polycations, composed of a polyamidoamine dendron head and a poly(l-lysine) tail (PAMAM dendron-PLL), through the introduction of disulfide bonds between the PLL tails. Disulfide bonds were successfully introduced through the reaction of Lys residues in the PAMAM dendron-PLL polymer vesicles with 2-iminothiolane. The stabilization of PAMAM dendron-PLL polymer vesicles was confirmed by dynamic light scattering measurements. In acid-base titration experiments, nanocapsules cross-linked by disulfide bonds had a buffering effect during the cellular uptake process. The PAMAM dendron-PLL nanocapsules were used to incorporate the fluorescent dyes rhodamine 6G and fluorescein as a drug model. Cationic rhodamine 6G was generally not released from the nanocapsules because of the electrostatic barrier of the PLL membrane. However, the nanocapsules were destabilized at high glutathione concentrations corresponding to intracellular concentrations. Rhodamine 6G was immediately released from the nanocapsules because of destabilization upon the cleavage of disulfide bonds. This release of rhodamine 6G from the nanocapsules was also observed in HeLa cells by laser confocal microscopy.

Highlights

  • The self-assembly of macromolecules is often used as an indispensable molecular tool in functional nanomaterial engineering [1,2,3,4,5,6,7]

  • Block copolymer-based micelles and vesicles with intracellular environment- responsive behaviors are of special interest for drug delivery system (DDS) carriers [8,9,10,11,12]

  • Lys residues in the PLL tails of PAMAM dendron-PLL polymer vesicles by a reaction between Lys residues and 2-iminothiolane (IT)

Read more

Summary

Introduction

The self-assembly of macromolecules is often used as an indispensable molecular tool in functional nanomaterial engineering [1,2,3,4,5,6,7]. Polymer micelles containing disulfide cross-linkages within the core have been reported to show effective destabilization in drug delivery They should be stable in the extracellular environment and promptly release the entrapped drug within the target cell upon the cleavage of disulfide bonds. Disulfide bonds can cleave in a reductive environment in cytoplasm, and PAMAM dendron-PLL nanocapsules will be destabilized under these conditions. These properties indicate that PAMAM dendron-PLL nanocapsules that are cross-linked by disulfide bonds can function as carriers in DDS. The release of rhodamine 6G in cytoplasm was confirmed by laser confocal microscopy These features of PAMAM dendron-PLL nanocapsules cross-linked by disulfide bonds can be used for effective drug delivery in the future

Preparation of Nanocapsules Stabilized by Disulfide Bonds
Release of Model Compounds from Nanocapsules and Cytotoxicity of Nanocapsules
Response of Nanocapsules to a Reductive Environment
Materials
Preparation of Nanocapsules Cross-Linked by Disulfide Bonds
Dye Release Experiments from Nanocapsules
In vitro Cytotoxicity and Laser Confocal Microscope Observations
Conclusions
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call