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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Freeze-dried chitosan nanoparticles to stabilize and deliver bromelain

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Autor(es):
Ataide, Janaina Artem [1] ; Geraldes, Danilo Costa [2] ; Gerios, Eloah Favero [3] ; Bissaco, Fernanda Mazon [3] ; Cefali, Leticia Caramori [2] ; Oliveira-Nascimento, Laura [3] ; Mazzola, Priscila Gava [3]
Número total de Autores: 7
Afiliação do(s) autor(es):
[1] Univ Campinas UNICAMP, Sch Med Sci, Grad Program Med Sci, Campinas - Brazil
[2] State Univ Campinas UNICAMP, Inst Biol, Grad Program Biosci & Technol Bioact Prod, Campinas - Brazil
[3] Univ Campinas UNICAMP, Fac Pharmaceut Sci, Candido Portinari St 200, Cidade Univ Zeferino Vaz, BR-13083871 Campinas - Brazil
Número total de Afiliações: 3
Tipo de documento: Artigo Científico
Fonte: JOURNAL OF DRUG DELIVERY SCIENCE AND TECHNOLOGY; v. 61, FEB 2021.
Citações Web of Science: 1
Resumo

Bromelain has many therapeutic properties including wound healing and blood circulation improvement. However, bromelain is usually unstable and suffers autolysis, which results in a decrease of enzymatic activity and limited applications. Encapsulation of bromelain in nanoparticles can diminish degradation by protease immobilization, which may increase its stability and efficacy. The natural polymer chitosan can be nanostructured and trap the enzyme, maintaining the claims of biocompatibility, biodegradability and natural source of the formulation ingredients. Considering the above, chitosan-bromelain nanoparticles (C-B-NP) were produced by ionic crosslinking and presented spherical shape (electron microscopy) of 100.9 +/- 0.5 nm and polydispersity index of 0.222 +/- 0.012 (dynamic light scattering). Encapsulation efficiency was calculated as 85.1 +/- 1% with regard to enzymatic activity, and C-B-NP presented 4.9 U/mL of enzymatic activity, which corresponds to 104.7% of free bromelain activity, confirming its integrity upon encapsulation. However, C-B-NP were unstable when stored in aqueous suspension, leading to freeze-drying studies of the formulation. Glycine and maltose were used as potential lyoprotectors and the formulation optimized by a factorial design; resultant products presented short resuspension time, slightly altered nanoparticles mean size and increased encapsulation rate compared to the previous liquid form. Maltose was able to better maintain formulation's enzymatic activity over time (90 days), especially when stored under refrigeration. Therefore, freeze-dried C-B-NP can effectively improve bromelain and nanoparticle stability, which allow further in vivo applications as a dried powder for topical administration or as a raw material for other dosage forms. (AU)

Processo FAPESP: 16/02282-1 - Estudo da estabilidade e liberação de bromelina encapsulada em nanopartículas de quitosana
Beneficiário:Eloah Favero Gérios
Modalidade de apoio: Bolsas no Brasil - Iniciação Científica
Processo FAPESP: 16/02287-3 - Encapsulação de bromelina em nanopartículas de quitosana
Beneficiário:Fernanda Mazon Bissaco
Modalidade de apoio: Bolsas no Brasil - Iniciação Científica
Processo FAPESP: 16/03444-5 - Desenvolvimento de formulação farmacêutica cicatrizante contendo bromelina extraída de resíduos industriais
Beneficiário:Priscila Gava Mazzola
Modalidade de apoio: Auxílio à Pesquisa - Regular
Processo FAPESP: 15/15068-5 - Desenvolvimento de partículas poliméricas como sistemas carreadores de produto bioativo
Beneficiário:Janaína Artem Ataide
Modalidade de apoio: Bolsas no Brasil - Mestrado