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Formulation and Characterization of Triamcinolone Acetonide Acetate-Loaded Microspheres Prepared by a Static Mixing Technique.
Du, Huan-Huan; Wang, Li-Rong; Wu, Xin-Hong; Liu, Xue-Ai; Huo, Ming-Wei; Huang, Xiang-Xiang; Shi, Ling-Zhi; Liu, Yawen; Tang, Min; Shi, Li-Li; Cao, Qing-Ri.
Afiliação
  • Du HH; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Wang LR; Huaguoshan Medical Science Center, Lianyungang Economic & Technological Development Area, Lianyungang, People's Republic of China.
  • Wu XH; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Liu XA; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Huo MW; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Huang XX; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Shi LZ; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Liu Y; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Tang M; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
  • Shi LL; School of Food and Pharmacy, Zhejiang Ocean University, Zhoushan, People's Republic of China.
  • Cao QR; College of Pharmaceutical Sciences, Soochow University, Suzhou, People's Republic of China.
Curr Drug Deliv ; 2024 Jun 05.
Article em En | MEDLINE | ID: mdl-38847256
ABSTRACT

PURPOSE:

Reproducibility and scale-up production of microspheres through spray drying present significant challenges. In this study, biodegradable microspheres of Triamcinolone Acetonide Acetate (TAA) were prepared using a novel static mixing method by employing poly( lactic-co-glycolic acid) (PLGA) as the sustained-release carrier.

METHODS:

TAA-loaded microspheres (TAA-MSs) were prepared using a static mixing technique. The PLGA concentration, polyvinyl alcohol concentration (PVA), phase ratio of oil/water, and phase ratio of water/solidification were optimized in terms of the particle size, drug loading (DL), and encapsulation efficiency (EE) of TAA-MSs. The morphology of TAA-MSs was examined using Scanning Electron Microscopy (SEM), while the physicochemical properties were evaluated through X-ray diffraction (XRD), Differential Scanning Calorimetry (DSC), and Fourier Transform Infrared Spectroscopy (FT-IR). The in vitro release of TAA-MSs was compared to that of the pure drug (TAA) using a water-bath vibration method in the medium of pH 7.4 at 37°C.

RESULTS:

The formulation composition and preparation condition for the preparation of TAA-MSs were optimized as follows the PLGA concentration was 1%, the phase ratio of oil(dichloromethane) /water (PVA solution) was 13, the phase ratio of water (PVA solution)/solidification was 12. The optimized TAA-MSs displayed spherical particles with a size range of 30-70 µm, and DL and EE values of 27.09% and 98.67%, respectively. Moreover, the drug-loaded microspheres exhibited a significant, sustained release, with 20% of the drug released over a period of 28 days. The XRD result indicated that the crystalline form of TAA in microspheres had been partly converted into the amorphous form. DSC and FT-IR results revealed that some interactions between TAA and PLGA occurred, indicating that the drug was effectively encapsulated into PLGA microspheres.

CONCLUSION:

TAA-loaded PLGA microspheres have been successfully prepared via the static mixing technique with enhanced EE and sustained-release manner.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Curr Drug Deliv / Curr. drug deliv / Current drug delivery Assunto da revista: FARMACIA / FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Curr Drug Deliv / Curr. drug deliv / Current drug delivery Assunto da revista: FARMACIA / FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2024 Tipo de documento: Article
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