Dual Functional Microcapsule based on Monodisperse Short PEG Amphiphile for Drug Encapsulation and Protein Affinity Controlled Release

Author:

Ketkar Rohit N.1ORCID,Dey Paritosh1,Sodnawar Triveni2,Sharma Shilpy2,M Manikandan3,Dutta Choudhury Sharmistha45,Sadhukhan Nabanita1ORCID

Affiliation:

1. Department of Speciality Chemicals Technology Institute of Chemical Technology Matunga (E) Mumbai Maharashtra 400019 India

2. Department of Biotechnology Savitribai Phule Pune University Ganeshkind Road Pune Maharashtra 411007 India

3. Medicinal Chemistry and Cell Biology Laboratory Department of Chemical Sciences Tata Institute of Fundamental Research Homi Bhabha Road Mumbai Maharashtra 400005 India

4. Bhabha Atomic Research Centre Mumbai 400085 India.

5. Homi Bhabha National Institute Anushaktinagar Mumbai 400094 India

Abstract

AbstractA short monodisperse poly(ethylene glycol) (PEG) and a neutral organic rotamer conjugate TEG‐BTA‐2 amphiphile was designed for the construction of a stimuli‐responsive switchable self‐assembled structure for drug encapsulation by noncovalent interaction and targeted controlled delivery. A short PEG, tetraethylene glycol (TEG) was covalently attached with a neutral organic rotamer benzothiazole dye (BTA‐2) affording the neutral TEG‐BTA‐2 (<500 D). The TEG‐BTA‐2 is self‐assembled into a microsphere in an aqueous medium, but remarkably undergoes morphology change switching to a rice‐like microcapsule for curcumin encapsulation. Curcumin‐loaded microcapsules were stable in an aqueous solution, however, were noticed disintegrating upon the addition of BSA protein. This is possibly due to an interaction with BSA protein leading to a protein affinity‐controlled curcumin release in a neutral PBS buffer. Moreover, cell internalization of the neutral amphiphile TEG‐BTA‐2 into A549 cells was observed by fluorescence microscopy, providing an opportunity for application as a molecular vehicle for targeted drug delivery and monitoring.

Publisher

Wiley

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