Mucoadhesive nanoparticles-based oral drug delivery systems enhance ameliorative effects of low molecular weight heparin on experimental colitis

被引:50
作者
Yan, Yan [1 ,2 ]
Sun, Ying [2 ]
Wang, Pengchong [1 ,2 ]
Zhang, Rui [2 ]
Huo, Chuanchuan [2 ]
Gao, Tingting [2 ]
Song, Chenghua [3 ]
Xing, Jianfeng [2 ]
Dong, Yalin [1 ]
机构
[1] Xi An Jiao Tong Univ, Affiliated Hosp 1, Dept Pharm, 277 Yanta West Rd, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Pharm, Dept Pharmaceut, Xian, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Affiliated Hosp 1, Shaanxi Prov Ctr Regenerat Med & Surg Engn, Natl Local Joint Engn Res Ctr Precis Surg & Regen, Xian, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Ulcerative colitis; Low molecular weight heparin; Trimethyl chitosan; Mucoadhesion; Colon targeting; Oral drug delivery; IN-VIVO EVALUATION; ULCERATIVE-COLITIS; CHITOSAN; VITRO; QUATERNIZATION; MICROPARTICLES; ABSORPTION; DISEASE; ACID; RAT;
D O I
10.1016/j.carbpol.2020.116660
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Low molecular weight heparin (LMWH) is reported to have therapeutic action on ulcerative colitis (UC). To facilitate its oral administration and improve the colon-targeting property, LMWH-loaded nanoparticles (TMC-NPs and SA-TMC-NPs) are prepared and evaluated by a series of studies, including their stabilities, drug release profiles, mucosal permeation, mucoadhesion, cytotoxicities, cellular uptake profiles, anticoagulant and anti-inflammatory activities, mucosal healing properties, biosafety and ameliorative effects on experimental colitis. Consequently, oral administration of LMWH-loaded NPs for 5 days perform significant therapeutic effects on mice, which are manifested as improved body weight gains, colon length, DAI score, MPO activity and histological characteristics. Besides, SA-TMC-NPs show better colon-targeting property than TMC-NPs that is demonstrated by lower oral absorption (ATPP 38.95 s) and stronger mucoadhesion (kcps reduces 36.46 %) to inflamed colon tissues. Therefore, TMC-based NPs are proved to be as promising oral colon-targeting drug delivery systems of LMWH and has potential application in UC treatment.
引用
收藏
页数:12
相关论文
共 38 条
[1]   Alginate microparticles as oral colon drug delivery device: A review [J].
Aguero, Lissette ;
Zaldivar-Silva, Dionisio ;
Pena, Luis ;
Dias, Marcos L. .
CARBOHYDRATE POLYMERS, 2017, 168 :32-43
[2]   Chitosan-based delivery systems for protein therapeutics and antigens [J].
Amidi, Maryam ;
Mastrobattista, Enrico ;
Jiskoot, Wim ;
Hennink, Wim E. .
ADVANCED DRUG DELIVERY REVIEWS, 2010, 62 (01) :59-82
[3]   Alginate coated chitosan core shell nanoparticles for oral delivery of enoxaparin: In vitro and in vivo assessment [J].
Bagre, Archana Pataskar ;
Jain, Keerti ;
Jain, Narendra K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2013, 456 (01) :31-40
[4]   Chitosan and chitosan ethylene oxide propylene oxide block copolymer nanoparticles as novel carriers for proteins and vaccines [J].
Calvo, P ;
RemunanLopez, C ;
VilaJato, JL ;
Alonso, MJ .
PHARMACEUTICAL RESEARCH, 1997, 14 (10) :1431-1436
[5]   Efficacy of Intracolonic Administration of Low-Molecular-Weight Heparin CB-01-05, Compared to Other Low-Molecular-Weight Heparins and Unfractionated Heparin, in Experimentally Induced Colitis in Rat [J].
Celasco, Giuseppe ;
Moro, Luigi ;
Bozzella, Roberta ;
Mangano, Katia ;
Quattrocchi, Cinzia ;
Aiello, Caterina ;
Donia, Marco ;
Fagone, Paolo ;
Di Marco, Roberto .
DIGESTIVE DISEASES AND SCIENCES, 2008, 53 (12) :3170-3175
[6]   Recent advances in chitosan-based nanoparticles for oral delivery of macromolecules [J].
Chen, Mei-Chin ;
Mi, Fwu-Long ;
Liao, Zi-Xian ;
Hsiao, Chun-Wen ;
Sonaje, Kiran ;
Chung, Min-Fan ;
Hsu, Li-Wen ;
Sung, Hsing-Wen .
ADVANCED DRUG DELIVERY REVIEWS, 2013, 65 (06) :865-879
[7]   pH-responsive thiolated chitosan nanoparticles for oral low-molecular weight heparin delivery: in vitro and in vivo evaluation [J].
Fan, Bo ;
Xing, Yang ;
Zheng, Ying ;
Sun, Chuan ;
Liang, Guixian .
DRUG DELIVERY, 2016, 23 (01) :238-247
[8]   Ulcerative colitis [J].
Ungaro, Ryan ;
Mehandru, Saurabh ;
Allen, Patrick B. ;
Peyrin-Biroulet, Laurent ;
Colombel, Jean-Frederic .
LANCET, 2017, 389 (10080) :1756-1770
[9]   Effect of the degree of quaternisation of N-trimethyl chitosan chloride on absorption enhancement:: in vivo evaluation in rat nasal epithelia [J].
Hamman, JH ;
Stander, M ;
Kotzé, AF .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 232 (1-2) :235-242
[10]   Effect of the type of base and number of reaction steps on the degree of quaternization and molecular weight of N-trimethyl chitosan chloride [J].
Hamman, JH ;
Kotzé, AF .
DRUG DEVELOPMENT AND INDUSTRIAL PHARMACY, 2001, 27 (05) :373-380