evelopment of PEG-PCL-based polymersomes through design of experiments for co-encapsulation of vemurafenib and doxorubicin as chemotherapeutic drug

Autor(es)

D'Angelo, Natalia A. ^[1] ; Camara, Mayra C. C. ^[1] ; Noronha, Mariana A. ^[1] ; Grotto, Denise ^[2] ; Chorilli, Marlus ^[3] ; Lourenco, Felipe R. ^[4] ; Rangel-Yagui, Carlota De O. ^[5] ; Lopes, Andre M. ^[1]

Afiliação do(s) autor(es)

^[1] Univ Estadual Campinas, Fac Pharmaceut Sci, Campinas - Brazil

^[2] Univ Sorocaba, Sorocaba - Brazil

^[3] Sao Paulo State Univ UNESP, Sch Pharmaceut Sci, Dept Drugs & Med, Araraquara, SP - Brazil

^[4] Univ Sao Paulo, Sch Pharmaceut Sci, Dept Pharm, Sao Paulo - Brazil

^[5] Univ Sao Paulo, Sch Pharmaceut Sci, Dept Biochem & Pharmaceut Technol, Sao Paulo - Brazil

• Tipo de documento: Artigo Científico
• Fonte: JOURNAL OF MOLECULAR LIQUIDS; v. 349, MAR 1 2022.
• Citações Web of Science: 0

Resumo

Nanostructures for co-encapsulation of chemotherapeutic drugs have been widely studied for the last years due to its important advantages, e.g. improved bioavailability and cellular uptake, increased solubility of drugs, and lower chances of multidrug resistance (MDR). In this context, this work describes essential parameters of production and characterization of poly(ethylene glycol)-block-poly(epsilon-caprolactone) (PEG-PCL)-based polymersomes (Ps) for the co-encapsulation of two chemotherapeutic drugs, doxorubicin (DOX) and vemurafenib (VEM). Three PEG-PCL copolymers were studied, namely PEG(45)PCL(44), PEG(114)PCL(98), and PEG(114)PCL(114). We evaluated the effect of conditions such as stirring speed, stirring time, hydration volume, and ultrasound time in particle size (D-H) and polydispersity index (PDI) by two statistical designs (2(3)) to achieve improved (smaller) D-H and PDI of PEG-PCL-based Ps. According to our results, the best condition to generate PEG-PCL-based Ps was to employ 1050 rpm of stirring speed by 42 h, a hydration volume of 15 mL (0.05% m/v), and ultrasound by 35 min, resulting in a D-H and PDI range of 210 to 245 nm and 0.117 to 0.148, respectively. Moreover, co-encapsulation of DOX and VEM resulted in drug loading ranges of 12 to 18% and 16 to 26% and encapsulation efficiency of 35 to 39% and 43 to 55%, for DOX and VEM, respectively, together with an increase in the D-H (i.e., 254 to 282 nm). The Ps nanoformulations were stable at 4, 25, and 37 degrees C and the release of drugs was faster with the smaller PEG-PCL blocks (i.e., PEG(45)PCL(44) > PEG(114)PCL(98) > PEG(114)PCL(114)). The PEG-PCL-based Ps also demonstrated higher drugs release in an acidic environment (i.e., pH 5.0 at 37 degrees C, found in tumor cells) compared to physiological conditions (pH 7.4 at 37 degrees C). In conclusion, the DOX/VEM-PEG-PCL-based Ps may be a promising approach to cancer therapy with potential synergic effect, lower dosage, and lower risk of causing MDR. (C) 2021 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 17/10789-1 - Terapia combinatória utilizando polimerossomos decorados com transferrina e incorporados em hidrogéis de quitosana como smart drug delivery systems para células tumorais de melanoma
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• Modalidade de apoio: Bolsas no Brasil - Jovens Pesquisadores
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