Temperature-sensitive lyotropic liquid crystals as systems for transdermal drug delivery

被引:16
|
作者
Liu, Jinpeng [1 ,3 ]
Cheng, Ranran [1 ,3 ]
Heimann, Kirsten [2 ,3 ]
Wang, Zhongni [4 ]
Wang, Jinying [1 ,3 ]
Liu, Feng [1 ,3 ]
机构
[1] Qilu Univ Technol, Sch Pharmaceut Sci, Shandong Acad Sci, Jinan 250014, Shandong, Peoples R China
[2] Flinders Univ S Australia, Coll Med & Publ Hlth, Ctr Marine Bioprod Dev, Adelaide, SA 5042, Australia
[3] Qilu Univ Technol, Key Lab Appl Technol Sophisticated Analyt Instrum, China Australia Joint Lab Nat Bioresource Ind Inn, Shandong Anal & Test Ctr,Shandong Acad Sci, Jinan 250014, Shandong, Peoples R China
[4] Shandong Normal Univ, Coll Chem Chem Engn & Mat Sci, Jinan 250014, Peoples R China
关键词
Lyotropic liquid crystals; Temperature sensitive; Phase transition; Transdermal drug delivery; IN-VITRO RELEASE; PHASE-BEHAVIOR; CUBIC PHASE; NANO-EMULSIFICATION; OIL; MICROSTRUCTURE; WATER; ACID; BIOAVAILABILITY; NANOEMULSIONS;
D O I
10.1016/j.molliq.2021.115310
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The purpose of this study was to develop temperature-sensitive lyotropic liquid crystals (LLC) for transdermal drug delivery systems. The hexagonal and cubic LLC samples were constructed in the polyoxyethylene (20) sorbitan monooleate (Tween 80)/PEG-60 hydrogenated castor oil (RH 60)/Ethyl oleate (EtOL)/water (H2O) system and characterized by Small Angle X-ray Scattering (SAXS), low field nuclear magnetic resonance (LF-NMR) and rheology. Additionally, its skin permeation behavior in vitro and cell-stimulating studies were investigated as well. The LLC system exhibited temperature sensitivity. Under the influence of temperature, the structure of LLC collapsed and was transformed into micellar solution. While, sample S-3 (water content was 35 wt%.) was transformed from cubic LLC to hexagonal LLC then to micellar solution as temperature increased. The compositions and the introduction of paeonol both can influence the structure of LLC, and were used to adjust the phase transition temperature to close to the human body temperature. In vitro transdermal experiments showed that the release behavior of paeonol-loaded LLC was obviously temperature-sensitive and controlled by concentration diffusion. In vitro cell-stimulating studies displayed that LLC samples exhibited no obvious toxicity. The above results indicated that the temperature-sensitive LLC had potential to be applied as a transdermal drug delivery system. (C) 2021 Elsevier B.V. All rights reserved.
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页数:8
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