Development of novel pH-sensitive thiolated chitosan/PMLA nanoparticles for amoxicillin delivery to treat Helicobacter pylori

被引:74
作者
Arif, Muhammad [1 ]
Dong, Quan-Jiang [2 ]
Raja, Mazhar Ali [1 ]
Zeenat, Shah [1 ]
Chi, Zhe [1 ]
Liu, Chen-Guang [1 ]
机构
[1] Ocean Univ China, Coll Marine Life Sci, 5 Yushan Rd, Qingdao 266003, Shandong, Peoples R China
[2] Qingdao Municipal Hosp, Dept Gastroenterol, Cent Labs, Qingdao 266000, Shandong, Peoples R China
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2018年 / 83卷
关键词
Helicobacter pylori; Chitosan; Poly (malic acid) (PMLA); Mucoadhesive; Multifunctional nanoparticles; pH-sensitive; Targeted delivery; SELF-ASSEMBLED NANOPARTICLES; ANTIBACTERIAL APPLICATIONS; ANTIMICROBIAL POLYMERS; DRUG-DELIVERY; THERAPY; ERADICATION; ACID; MICROSPHERES; HYDROGELS; THIOMERS;
D O I
10.1016/j.msec.2017.08.038
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
The cysteine conjugated chitosan/PMLA multifunctional nanoparticles were synthesized as targeted Nano-drug delivery system to eradicate Helicobacter pylori. Helicobacter pylori specifically express urea transport protein on its membrane to carrying urea to the cytoplasm urease to supply ammonia that protects bacteria in the acid environment of the stomach. The clinical suitability of topical antimicrobial agents is required to get rid of Helicobacter pylori inside the inflamed basal region. In this work, cysteine conjugated chitosan derivative, Cys-CS for their mucoadhesive and anticoagxilant properties was designed and synthesized, for the preparation of multifunctional nanoparticles. The technique turned into optimized to prepare Cys-CS/PMLA nanoparticles for encapsulation of amoxicillin. The results showed that amoxkillin-Cys-CS/PMLA nanoparticles exhibit favorable pH-sensitive properties that could procrastinate the release of amoxicillin at gastric acid and allow the drug to deliver and target to Helicobacter pylori at its survival region efficiently. In comparison with unmodified amoxicillin-chitosan/PMLA nanoparticles, effective inhibition of Helicobacter pylori growth was observed for amoxicillin-Cys-CS/PMLA nanoparticles. These results indicate that the multifunctional amoxicillin-loaded nanoparticles have great potential for the effective treatment of Helicobacter pylori infection. They can also be used as pharmacologically powerful nanocarriers for oral targeted delivery of different therapeutic drugs to treat Helicobacter pylori.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 45 条
[1]   Preparation and characterization of polyelectrolyte complex nanoparticles based on poly (malic acid), chitosan. A pH-dependent delivery system [J].
Arif, Muhammad ;
Raja, Mazhar Ali ;
Zeenat, Shah ;
Chi, Zhe ;
Liu, Chenguang .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2017, 28 (01) :50-62
[2]  
Bendcop-Schniirch A., 2004, EUR J PHARM BIOPHARM, V57, P9
[3]   Thiomers:: potential excipients for non-invasive peptide delivery systems [J].
Bernkop-Schnürch, A ;
Krauland, AH ;
Leitner, VM ;
Palmberger, T .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2004, 58 (02) :253-263
[4]   Nanoparticles Incorporated in pH-Sensitive Hydrogels as Amoxicillin Delivery for Eradication of Helicobacter pylori [J].
Chang, Chiung-Hung ;
Lin, Yu-Hsin ;
Yeh, Chia-Lin ;
Chen, Yi-Chi ;
Chiou, Shu-Fen ;
Hsu, Yuan-Man ;
Chen, Yueh-Sheng ;
Wang, Chi-Chung .
BIOMACROMOLECULES, 2010, 11 (01) :133-142
[5]   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
[6]   Chemical characteristics of O-carboxymethyl chitosans related to the preparation conditions [J].
Chen, XG ;
Park, HJ .
CARBOHYDRATE POLYMERS, 2003, 53 (04) :355-359
[7]   Poly(β-L-malic acid) (PMLA) from Aureobasidium spp. and its current proceedings [J].
Chi, Zhe ;
Liu, Guang-Lei ;
Liu, Chen-Guang ;
Chi, Zhen-Ming .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2016, 100 (09) :3841-3851
[8]   Cationic Polymers and their Self-Assembly for Antibacterial Applications [J].
Deka, Smriti Rekha ;
Sharma, Ashwani Kumar ;
Kumar, Pradeep .
CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2015, 15 (13) :1179-1195
[9]   Bio-inspired crosslinking and matrix-drug interactions for advanced wound dressings with long-term antimicrobial activity [J].
Dhand, Chetna ;
Venkatesh, Mayandi ;
Barathi, Veluchami Amutha ;
Harini, Sriram ;
Bairagi, Samiran ;
Leng, Eunice Goh Tze ;
Muruganandham, Nandhakumar ;
Low, Kenny Zhi Wei ;
Fazil, Mobashar Hussain Urf Turabe ;
Loh, Xian Jun ;
Srinivasan, Dinesh Kumar ;
Liu, Shou Ping ;
Beuerman, Roger W. ;
Verma, Navin Kumar ;
Ramakrishna, Seeram ;
Lakshminarayanan, Rajamani .
BIOMATERIALS, 2017, 138 :153-168
[10]   Emerging trends in macromolecular antimicrobials to fight multi-drug-resistant infections [J].
Engler, Amanda C. ;
Wiradharma, Nikken ;
Ong, Zhan Yuin ;
Coady, Daniel J. ;
Hedrick, James L. ;
Yang, Yi-Yan .
NANO TODAY, 2012, 7 (03) :201-222