Macromolecular confinement of therapeutic protein in polymeric particles for controlled release: insulin as a case study

ABSTRACT Sustained release systems for therapeutic proteins have been widely studied targeting to improve the action of these drugs. Molecular entrapping of proteins is particularly challenging due to their conformational instability. We have developed a micro-structured poly-epsilon-caprolactone (P...

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Main Authors: Luiz Henrique Guerreiro (Author), Daniel da Silva (Author), Wendell Girard-Dias (Author), Camile Moreira Mascarenhas (Author), Kildare Miranda (Author), Mauro Sola-Penna (Author), Eduardo Ricci Júnior (Author), Luís Mauricio Trambaioli da Rocha e Lima (Author)
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Published: Universidade de São Paulo, 2017-06-01T00:00:00Z.
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100 1 0 |a Luiz Henrique Guerreiro  |e author 
700 1 0 |a Daniel da Silva  |e author 
700 1 0 |a Wendell Girard-Dias  |e author 
700 1 0 |a Camile Moreira Mascarenhas  |e author 
700 1 0 |a Kildare Miranda  |e author 
700 1 0 |a Mauro Sola-Penna  |e author 
700 1 0 |a Eduardo Ricci Júnior  |e author 
700 1 0 |a Luís Mauricio Trambaioli da Rocha e Lima  |e author 
245 0 0 |a Macromolecular confinement of therapeutic protein in polymeric particles for controlled release: insulin as a case study 
260 |b Universidade de São Paulo,   |c 2017-06-01T00:00:00Z. 
500 |a 2175-9790 
500 |a 10.1590/s2175-97902017000216039 
520 |a ABSTRACT Sustained release systems for therapeutic proteins have been widely studied targeting to improve the action of these drugs. Molecular entrapping of proteins is particularly challenging due to their conformational instability. We have developed a micro-structured poly-epsilon-caprolactone (PCL) particle system loaded with human insulin using a simple double-emulsion w/o/w method followed by solvent evaporation method. This formulation is comprised by spheric-shaped microparticles with average size of 10 micrometers. In vitro release showed a biphasic behavior such as a rapid release with about 50% of drug delivered within 2 hours and a sustained phase for up to 48 h. The subcutaneous administration of microencapsulated insulin showed a biphasic effect on glycemia in streptozotocin-induced diabetic mice, compatible with short and intermediate-acting behaviors, with first transition peak at about 2 h and the second phase exerting effect for up to 48h after s.c. administration. This study reveals that a simplified double-emulsion system results in biocompatible human-insulin-loaded PCL microparticles that might be used for further development of optimized sustained release formulations of insulin to be used in the restoration of hormonal levels. 
546 |a EN 
690 |a Human insulin/study 
690 |a Microparticles 
690 |a Poly-ε-caprolactone 
690 |a Therapeutic proteins/study/action 
690 |a Proteins/molecular entrapping 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Brazilian Journal of Pharmaceutical Sciences, Vol 53, Iss 2 (2017) 
787 0 |n http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1984-82502017000200622&lng=en&tlng=en 
787 0 |n https://doaj.org/toc/2175-9790 
856 4 1 |u https://doaj.org/article/64f3cea23f8a44c6a1c7f5ea021b7f98  |z Connect to this object online.