Multi-functional pH-responsive and biomimetic chitosan-based nanoplexes for targeted delivery of ciprofloxacin against bacterial sepsis

被引:0
|
作者
Ismail, Eman A. [1 ,2 ]
Omolo, Calvin A. [1 ,3 ]
Gafar, Mohammed A. [1 ]
Khan, Rene [4 ]
Nyandoro, Vincent O. [1 ]
Salifu, Elliasu Y. [5 ]
Govender, Thirumala [1 ,6 ]
机构
[1] Univ KwaZulu Natal, Coll Hlth Sci, Discipline Pharmaceut Sci, Private Bag X54001, Durban, South Africa
[2] Univ Gezira, Fac Pharm, Dept Pharmaceut, Wad Madani, Sudan
[3] United States Int Univ Africa, Sch Pharm & Hlth Sci, Dept Pharmaceut, POB 14634-00800, Nairobi, Kenya
[4] Univ KwaZulu Natal, Coll Hlth Sci, Sch Lab Med & Med Sci, Discipline Med Biochem, Durban, South Africa
[5] South African Med Res Council SAMRC, Biomed Res & Innovat Platform BRIP, ZA-7505 Cape Town, South Africa
[6] United States Int Univ Africa, Sch Pharm & Hlth Sci, Dept Pharmaceut, POB 14634-00800, Nairobi 00800, Kenya
基金
英国医学研究理事会; 新加坡国家研究基金会;
关键词
Dual-functional; Chitosan; Nanoplexes; IN-VITRO CYTOTOXICITY; DRUG-DELIVERY; ANTIINFLAMMATORY ACTIVITY; HYALURONIC-ACID; NANOPARTICLES; FORMULATION; SYSTEMS; RELEASE; 5-FLUOROURACIL; INFECTIONS;
D O I
10.1016/j.ijbiomac.2024.130046
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial sepsis is a mortal syndromic disease characterized by a complex pathophysiology that hinders effective targeted therapy. This study aimed to develop multifunctional, biomimetic and pH-responsive ciprofloxacinloaded chitosan (CS)/sodium deoxycholic acid (SDC) nanoplexes (CS/SDC) nanoplexes with the ability to target and modulate the TLR4 pathway, activated during sepsis. The formulated nanoplexes were characterized in terms of physicochemical properties, in silico and in vitro potential biological activities. The optimal formulation showed good biocompatibility and stability with appropriate physicochemical parameters. The surface charge changed from negative at pH 7.4 to positive at pH 6.0 accompanied with a significantly faster release of CIP at pH 6.0 compared to 7.4. The biomimicry was elucidated by in silico tools and MST and results confirmed strong binding between the system and TLR4. Furthermore, the system revealed 4- and 2-fold antibacterial enhancement at acidic pH, and 3- and 4-fold better antibiofilm efficacy against Methicillin-resistant Staphylococcus aureus (MRSA) and Pseudomonas aeruginosa (P. aeruginosa) respectively, compared to bare CIP. In addition, enhanced bacterial efflux pump inhibition was demonstrated by CS/SDC nanoplexes. Finally, the developed nanosystem showed excellent antioxidant activity against DPPH radicals. Taken together, the study confirmed the multifunctionalities of CS/SDC nanoplexes and their potential benefits in improving bacterial sepsis therapy.
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页数:16
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