PMID- 31380250 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 2228-5881 (Print) IS - 2251-7308 (Electronic) IS - 2228-5881 (Linking) VI - 9 IP - 2 DP - 2019 Jun TI - Formulation and Physicochemical Characterization of Cyclosporine Microfiber by Electrospinning. PG - 249-254 LID - 10.15171/apb.2019.028 [doi] AB - Purpose: The objective of this study was to improve the permeability and water solubility rate of a poor water soluble drug, cyclosporine A (CsA). Methods: In order to improve the drug dissolution rate and oral bioavailability, electrospinning method was used as an approach to prepare. The fibers were evaluated for surface morphology, thermal characterizations, drug crystallinity, in vitro drug release and in vivo bioavailability studies. Results: Scanning electron microscope (SEM) results confirmed that the fibers were in microsize range and the size of the fibers was in the rang of 0.2 to 2 micron. Differential scanning calorimetry (DSC) and powder X-ray diffractometry (XRPD) analysis ensured that the crystalline lattice of drug were weakened or destroyed in the fibers. The drug release was 15.28%, 20.67%, and 32.84% from pure drug, fibers of formulation B, and formulation A, respectively. In vivo study results indicated that the bioavailability parameters of the optimized fiber formulation were improved and the maximum concentration (C(max)) were significantly higher for fibers (3001 ng/mL) than for pure drug (2550 ng/mL). The dissolution rate of the formulations was dependent on the nature and ratio of drug to carriers. Conclusion: The physicochemical properties showed that the optimized mixture of polyethylene glycol (PEG) and povidone (PVP) fibers could be an effective carrier for CsA delivery. PEG and PVP fibers improved the absolute bioavailability and drug dissolution rate with appropriate physicochemical properties. FAU - Mirzaeei, Shahla AU - Mirzaeei S AUID- ORCID: 0000-0002-1132-3150 AD - Pharmaceutical Sciences Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. FAU - Mohammadi, Ghobad AU - Mohammadi G AUID- ORCID: 0000-0002-6202-9840 AD - Pharmaceutical Sciences Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. FAU - Fattahi, Navid AU - Fattahi N AUID- ORCID: 0000-0002-5781-6700 AD - Student Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran. FAU - Mohammadi, Pardis AU - Mohammadi P AUID- ORCID: 0000-0002-4192-6737 AD - Pharmaceutical Sciences Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. FAU - Fattahi, Ali AU - Fattahi A AUID- ORCID: 0000-0001-8226-5835 AD - Pharmaceutical Sciences Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. FAU - Nikbakht, Mohammad Reza AU - Nikbakht MR AUID- ORCID: 0000-0001-7909-4967 AD - Pharmaceutical Sciences Research Center, School of Pharmacy, Kermanshah University of Medical Sciences, Kermanshah, Iran. FAU - Adibkia, Khosro AU - Adibkia K AUID- ORCID: 0000-0002-1053-5557 AD - Faculty of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran. LA - eng PT - Journal Article DEP - 20190601 PL - Iran TA - Adv Pharm Bull JT - Advanced pharmaceutical bulletin JID - 101578021 PMC - PMC6664123 OTO - NOTNLM OT - Bioavailability OT - Cyclosporine A OT - Electrospinning OT - Fibers OT - Polyethylene glycol OT - Povidone EDAT- 2019/08/06 06:00 MHDA- 2019/08/06 06:01 PMCR- 2019/06/01 CRDT- 2019/08/06 06:00 PHST- 2019/01/09 00:00 [received] PHST- 2019/04/28 00:00 [revised] PHST- 2019/05/02 00:00 [accepted] PHST- 2019/08/06 06:00 [entrez] PHST- 2019/08/06 06:00 [pubmed] PHST- 2019/08/06 06:01 [medline] PHST- 2019/06/01 00:00 [pmc-release] AID - 10.15171/apb.2019.028 [doi] PST - ppublish SO - Adv Pharm Bull. 2019 Jun;9(2):249-254. doi: 10.15171/apb.2019.028. Epub 2019 Jun 1.