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Synthesis and characterization of thiolated hexanoyl glycol chitosan as a mucoadhesive thermogelling polymer
被引:28
|作者:
Cho I.S.
[1
]
Oh H.M.
[1
]
Cho M.O.
[1
,2
]
Jang B.S.
[1
]
Cho J.-K.
[3
]
Park K.H.
[1
,2
]
Kang S.-W.
[2
,4
]
Huh K.M.
[1
]
机构:
[1] Department of Organic Materials Engineering, Chungnam National University, 99 Daehak-ro, Yuseong-gu, Daejeon
[2] Predictive Model Research Center, Korea Institute of Toxicology, 141, Gajeong-ro, Yuseong-gu, Daejeon
[3] Ezlab, 120, Heungdeokjungang-ro, Giheung-gu, Yongin-si, Gyeonggi-do
[4] Human and Environmental Toxicology Program, University of Science and Technology, 217, Gajeong-ro, Yuseong-gu, Daejeon
基金:
新加坡国家研究基金会;
关键词:
Chemical modification;
Hexanoyl glycol chitosan;
Mucoadhesive polymer;
Rheological measurements;
Thermogelling property;
Thiolation;
D O I:
10.1186/s40824-018-0137-7
中图分类号:
学科分类号:
摘要:
Background: Mucoadhesive polymers, which may increase the contact time between the polymer and the tissue, have been widely investigated for pharmaceutical formulations. In this study, we developed a new polysaccharidebased mucoadhesive polymer with thermogelling properties. Methods: Hexanoyl glycol chitosan (HGC), a new thermogelling polymer, was synthesized by the chemical modification of glycol chitosan using hexanoic anhydride. The HGC was further modified to include thiol groups to improve the mucoadhesive property of thermogelling HGC. The degree of thiolation of the thiolated HGCs (SHHGCs) was controlled in the range of 5-10% by adjusting the feed molar ratio. The structure of the chemically modified polymers was characterized by 1H NMR and ATR-FTIR. The sol-gel transition, mucoadhesiveness, and biocompatibility of the polymers were determined by a tube inverting method, rheological measurements, and in vitro cytotoxicity tests, respectively. Results: The aqueous solution (4 wt%) of HGC with approximately 33% substitution showed a sol-gel transition temperature of approximately 41 °C. SH-HGCs demonstrated lower sol-gel transition temperatures (34 ± 1 and 31 ± 1 °C) compared to that of HGC due to the introduction of thiol groups. Rheological studies of aqueous mixture solutions of SH-HGCs and mucin showed that SH-HGCs had stronger mucoadhesiveness than HGC due to the interaction between the thiol groups of SH-HGCs and mucin. Additionally, we confirmed that the thermogelling properties might improve the mucoadhesive force of polymers. Several in vitro cytotoxicity tests showed that SHHGCs showed little toxicity at concentrations of 0.1-1.0 wt%, indicating good biocompatibility of the polymers. Conclusions: The resultant thiolated hexanoyl glycol chitosans may play a crucial role in mucoadhesive applications in biomedical areas. © The Author(s).
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