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Indexed by:期刊论文
Date of Publication:2019-01-01
Journal:RSC ADVANCES
Included Journals:SCIE、Scopus
Volume:9
Issue:4
Page Number:2268-2276
ISSN No.:2046-2069
Key Words:Aggregates; Cellulose; High resolution transmission electron microscopy; Light scattering; Light transmission; Targeted drug delivery; Transmission electron microscopy, Amphotericin B; Cell viability; Confocal laser scanning microscopy; Critical aggregation concentration; Hydroxyethyl cellulose; Lower critical solution temperature; Thermo-responsive; Thermoresponsive polymer, Controlled drug delivery
Abstract:successfully synthesized, characterized, and applied for thermoresponsive drug delivery. The lower critical solution temperature (LCST) of HIPEC could be easily tuned from 21.1 to 56.1 degrees C as the molar substitution (MS) increased from 1.21 to 2.88. Dynamic light scattering and transmission electron microscopy experiments revealed that HIPEC can self-assemble into nano-sized aggregates, and their size could be changed by variation in temperature. Additionally, the critical aggregation concentration (CAC) ranged from 0.101 to 0.805 g L-1 by changing MS of HIPEC. In vitro drug delivery studies indicated that the amphotericin B (AmpB) release rate was much faster at temperatures above LCST; approximately 95% of the drug was released from aggregates in 40 h. MTT assays were conducted to evaluate the cytotoxicity of HIPEC, and the observation of the Hoechst 33342 living cell stain using confocal laser scanning microscopy confirmed the high cell viability as HIPECs were used.