A Quadruped Study on Chitosan Microspheres Containing Atorvastatin Calcium: Preparation, Characterization, Quantification and in-Vivo Application


Creative Commons License

EROĞLU H., NEMUTLU E., TURKOGLU O. F., NACAR O., BODUR E., SARGON M. F., ...More

CHEMICAL & PHARMACEUTICAL BULLETIN, vol.58, no.9, pp.1161-1167, 2010 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 58 Issue: 9
  • Publication Date: 2010
  • Doi Number: 10.1248/cpb.58.1161
  • Journal Name: CHEMICAL & PHARMACEUTICAL BULLETIN
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.1161-1167
  • Keywords: microsphere, chitosan, atorvastatin, spinal cord injury, quantification, SPINAL-CORD-INJURY, NITRIC-OXIDE SYNTHASE, INFLAMMATORY RESPONSE, MULTIPLE-SCLEROSIS, CONTROLLED-RELEASE, CEREBRAL-ISCHEMIA, CORTICAL-NEURONS, DELIVERY SYSTEM, STROKE, BRAIN
  • Hacettepe University Affiliated: Yes

Abstract

Atorvastatin is commonly used as a cholesterol lowering agent in patients. Recently, the neuroprotective effects of atorvastatin became the focus of many research studies. In this study, we have formulated chitosan microspheres containing atorvastatin calcium. In-vitro characterization of chitosan microspheres and quantification of atorvastatin calcium from formulations were also evaluated. The neuroprotective efficiency of atorvastatin calcium was investigated by an experimental spinal cord injury model. Atorvastatin calcium microspheres were implanted at the laminectomy area (1 mg/kg) immediately after trauma. Twenty-four hours after injury, motor functions of animals were scored according to modified Tarlov Scale. In spinal cord tissues tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-6 and lipid peroxidation levels were quantified and ultrastructural changes have been investigated. The results of all parameters indicate that microspheres containing atorvastatin calcium were capable of improving functional outcome, attenuating the expression of TNF-alpha, IL-1 beta and IL-6; lowering lipid peroxidation levels and maintaining the preservation of the cellular uniformity.