Fabrication and characterization of physically crosslinked alginate/ chitosan-based hydrogel loaded with neomycin for the treatment of skin infections caused by Staphylococcus aureus

被引:2
|
作者
Silva, Lucas dos Santos [1 ]
Nova, Beatriz Gomes Vila [1 ]
de Sousa, Carlos Eduardo Morais [1 ]
Silva, Raphael Guedes [1 ]
Carvalho, Layse Ribeiro de Sousa [1 ]
Silva, Izadora Souza Soeiro [1 ]
Moreira, Pedro Henrique de Aguiar [2 ]
Cardenas, Andres Felipe Millan [2 ]
Monteiro, Cristina de Andrade [3 ]
Tofanello, Aryane [4 ,5 ]
Garcia, Wanius [5 ]
Teixeira, Claudener Souza [6 ]
da Silva, Luis Claudio Nascimento [1 ]
机构
[1] Univ CEUMA, Nucleo Biomed, BR-65075120 Imperatriz, MA, Brazil
[2] Univ CEUMA, Lab Odontol, BR-65075120 Sao Luis, MA, Brazil
[3] Inst Fed Educ Ciencia & Tecnol Maranhao IFMA, Lab Pesquisa & Estudo Microbiol, BR-65030005 Sao Luis, Brazil
[4] Univ Presbiteriana Mackenzie, Ctr Adv Graphene Nanomat & Nanotechnol Res MackGra, Sao Paulo, SP, Brazil
[5] Univ Fed ABC, Ctr Ciencias Nat & Humanas CCNH, Santo Andre, SP, Brazil
[6] Univ Fed Cariri, Ctr Ciencias Agr & Biodiversidade, Juazeiro Do Norte, CE, Brazil
关键词
Polymeric formulation; Infected wounds; Biocompatible hydrogel;
D O I
10.1016/j.ijbiomac.2024.132577
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
Staphylococcus aureus is a pathogen widely involved in wound infection due to its ability to release several virulence factors that impair the skin healing process, as well as its mechanism of drug resistance. Herein, sodium alginate and chitosan were combined to produce a hydrogel for topical delivery of neomycin to combat S. aureus associated with skin complications. The hydrogel was formulated by combining sodium alginate (50 mg/mL) and chitosan (50 mg/mL) solutions in a ratio of 9:1 ( HBase ). Neomycin was added to HBase to achieve a concentration of 0.4 mg/mL ( HNeo ). The incorporation of neomycin into the product was confirmed by scanning electron microscopy, FTIR and TGA analysis. The hydrogels produced are homogeneous, have a high swelling capacity, and show biocompatibility using erythrocytes and fibroblasts as models. The formulations showed physicochemical and pharmacological stability for 60 days at 4 +/- 2 degrees C. HNeo totally inhibited the growth of S. aureus after 4 h. The antimicrobial effects were confirmed using ex vivo (porcine skin) and in vivo (murine) wound infection models. Furthermore, the HNeo- treated mice showed lower severity scores than those treated with HBase . Taken together, the obtained results present a new low-cost bioproduct with promising applications in treating infected wounds.
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页数:13
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