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Dr. Thavasyappan Thambi, Ph.D.
Assistant Professor | Department of Biotechnology, The University of Suwon


+82-10-3175-5458


Department of Biotechnology, College of Engineering

The University of Suwon, South Korea



Self-Assembled Amphiphilic Starch Based Drug Delivery Platform: Synthesis, Preparation, and Interactions with Biological Barriers.


Journal article


V. Phan, Huu Thuy Trang Duong, Phu-Tri Tran, Thavasyappan Thambi, Duy‐Khiet Ho, X. Murgia
Biomacromolecules, 2020

Semantic Scholar DOI PubMed
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APA   Click to copy
Phan, V., Duong, H. T. T., Tran, P.-T., Thambi, T., Ho, D. K., & Murgia, X. (2020). Self-Assembled Amphiphilic Starch Based Drug Delivery Platform: Synthesis, Preparation, and Interactions with Biological Barriers. Biomacromolecules.


Chicago/Turabian   Click to copy
Phan, V., Huu Thuy Trang Duong, Phu-Tri Tran, Thavasyappan Thambi, Duy‐Khiet Ho, and X. Murgia. “Self-Assembled Amphiphilic Starch Based Drug Delivery Platform: Synthesis, Preparation, and Interactions with Biological Barriers.” Biomacromolecules (2020).


MLA   Click to copy
Phan, V., et al. “Self-Assembled Amphiphilic Starch Based Drug Delivery Platform: Synthesis, Preparation, and Interactions with Biological Barriers.” Biomacromolecules, 2020.


BibTeX   Click to copy

@article{v2020a,
  title = {Self-Assembled Amphiphilic Starch Based Drug Delivery Platform: Synthesis, Preparation, and Interactions with Biological Barriers.},
  year = {2020},
  journal = {Biomacromolecules},
  author = {Phan, V. and Duong, Huu Thuy Trang and Tran, Phu-Tri and Thambi, Thavasyappan and Ho, Duy‐Khiet and Murgia, X.}
}

Abstract

Core-shell structured nanoparticles (NPs) render the simultaneous coloading capacity of both hydrophobic and hydrophilic drugs and may eventually enhance therapeutic efficacy. In this study, we employed a facile squalenoylation technology to synthesize a new amphiphilic starch derivative from partially oxidized starch, which self-assembled into core-shell starch NPs (StNPs) only at a squalenyl degree of substitution (DoS) of ∼1%. The StNPs characteristics could be tuned as the functions of the polymer molecular weight, DoS, and NPs concentration. The biopharmaceutical features of the StNPs, including colloidal stability, carrier properties, and biocompatibility, were carefully investigated. The interaction study between StNPs and mucin glycoproteins, the main organic component of mucus, revealed a moderate mucin interacting profile. Furthermore, the StNPs also showed good penetration through Pseudomonas aeruginosa biofilms. These results nominate StNPs as a versatile drug delivery platform with potential applications for mucosal drug delivery and the treatment of persistent infections.


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