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Updated: Sep 16, 2025

PLGA Nanoparticles Formed by Single- or Double-emulsion with Vitamin E-TPGS
Published on: December 27, 2013
Development of HLB-Adjustable Poly(γ-glutamic acid)-Vitamin E Conjugates as Enhanced TPGS Alternatives for Improved
Chujuan Huang1,2, Yuanyuan Lin2, Guanglin Lu2
1Department of Pharmacology and Department of Gastroenterology of the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou 310058, China.
Abstract:
d-α-tocopherol polyethylene glycol succinate (TPGS) is an FDA-approved polymeric solubilizer that is widely used in the pharmaceutical field; however, its limited solubilization capacity and high toxicity limit its wider application. Herein, a novel amphiphile─γ-PGAVE conjugate─was synthesized as a TPGS alternative by esterifying hydrophobic α-tocopherol (i.e., vitamin E; VE) to a hydrophilic γ-polyglutamic acid (γ-PGA) backbone. By achieving a tunable VE grafting ratio (2.5-13.5%) through varying the molar ratio of γ-PGA carboxyl groups to VE, the critical micelle concentration (CMC = 2.4-9.1 μg/mL) and hydrophilic-lipophilic balance (HLB = 4.45-13.39) could be controlled. Among the various γ-PGAVEs with differing graft ratios of VE, γ-PGAVE with a 2.5% grafting ratio (γ-PGAVE-2.5%) demonstrated superior solubilization capacity in aqueous environments. Additionally, antioxidant assays showed that γ-PGAVE-2.5% displayed an improved antioxidant capacity comparable to that of TPGS while exhibiting a significantly lower cytotoxicity. The enhanced biocompatibility and solubilization capability of γ-PGAVE-2.5% suggest that it could be a promising candidate for a range of applications, including food additives, dietary supplements, cosmetic ingredients, and pharmaceutical excipients.
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