High throughput microfluidics-based synthesis of PEGylated liposomes for precise size control and efficient drug encapsulation-Reference-Cited by-同舟云学术

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High throughput microfluidics-based synthesis of PEGylated liposomes for precise size control and efficient drug encapsulation

Published:2024-06 Issue: Volume:238 Page:113926
ISSN:0927-7765
Container-title:Colloids and Surfaces B: Biointerfaces
language:en
Short-container-title:Colloids and Surfaces B: Biointerfaces

Author:

Akar Shima^ORCID,Fardindoost Somayeh,Hoorfar Mina^ORCID

Funder

NSERC

Publisher

Elsevier BV

Reference51 articles.

1. Simultaneous encapsulation of hydrophilic and lipophilic molecules in liposomes of DSPC;Romero-Arrieta;Thermochim. Acta,2020

2. Modulation of the physicochemical state of interior agents to prepare controlled release liposomes;Wang;Colloids Surf. B Biointerfaces,2009

3. Hypoglycemic activity and oral bioavailability of insulin-loaded liposomes containing bile salts in rats: The effect of cholate type, particle size and administered dose;Niu;Eur. J. Pharm. Biopharm.,2012

4. A Review of Liposomes as a Drug Delivery System: Current Status of Approved Products, Regulatory Environments, and Future Perspectives;Liu;Molecules,2022

5. A.M. Hillery, “Supramolecular lipidic drug delivery systems: From laboratory to clinic A review of the recently introduced commercial liposomal and lipid-based formulations of amphotericin B,” 1997.

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