Synthesis and experimental study of a novel polymer/gene compound drug controlled release system for the treatment of erectile dysfunction / 中华男科学杂志
Zhonghua nankexue
; Zhonghua nankexue;(12): 771-775, 2013.
Article
em Zh
| WPRIM
| ID: wpr-268005
Biblioteca responsável:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To overcome the deficiency in the current therapies for erectile dysfunction (ED), we designed and synthesized a novel high-efficiency polymer/gene compound drug controlled release system and discussed the feasibility of pH and temperature dually sensitive injectable hydrogel in ED gene therapy.</p><p><b>METHODS</b>We synthesized optimal siRNA gene nanoparticles by characterizing the zeta potential of polylysine (PLL)/siRNA gene compounds, and established a pH and temperature dually sensitive injectable gene compound drug controlled release system via Schiffs reaction between glycol chitosan (GC) and benzaldehyde capped OHC-PEO-PPO-PEO-CHO. Then we demonstrated the sustained release of the system at different temperatures.</p><p><b>RESULTS</b>When the mass ratio of PLL to siRNA was 20:1, the zeta potential of the PLL/siRNA gene compound reached the peak (+23.5 mV) and the siRNA was encapsulated by PLL in the maximal degree. GC and OHC-PEO-PPO-PEO-CHO was crosslinked via benzoicimine reaction when environmental pH was changed from 5.5 to 7.4. The reslease of the siRNA encapsulated in this system kept at a low rate at 37 degrees C, significantly enhanced with the increase of the temperature to 60 degrees C, rising to (122.5 +/- 5.3) microg at 1 000 minutes as compared with (23.8 +/- 6.0) microg at 37 degrees C (P < 0.05).</p><p><b>CONCLUSION</b>The polymer/gene compound drug controlled release system was successfully synthesized, which improved the stability and capacity of gene carriers and achieved siRNA release at different temperatures, promising to be a new approach to the gene therapy of ED.</p>
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Base de dados:
WPRIM
Assunto principal:
Farmacologia
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Polilisina
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Polímeros
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Terapia Genética
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Química
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Sistemas de Liberação de Medicamentos
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Preparações de Ação Retardada
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RNA Interferente Pequeno
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Tratamento Farmacológico
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Nanopartículas
Limite:
Humans
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Male
Idioma:
Zh
Revista:
Zhonghua nankexue
Ano de publicação:
2013
Tipo de documento:
Article