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Physicochemical stability and aerosolization performance of dry powder inhalation system containing ciprofloxacin hydrochloride.
J Pharm Biomed Anal. 2018 Jan 30; 148:73-79.JP

Abstract

Antibiotic delivery in form of dry powder inhalation has been studied for possible clinical treatment of respiratory tract infection in the recent years. Dry powder inhalation of ciprofloxacin hydrochloride (CIP) assures local antibacterial activity and comfort of easy application. The aim of this work was to test the stability of co-spray-dried CIP in carrier free system. Since the microparticles in the dry powder system are amorphous and do not contain any stabilizer, the effects of temperature and relative humidity (RH) on the physicochemical properties and aerosolization behavior are very important. Therefore investigation of the role of excipients (such as polyvinyl alcohol (PVA), l-leucine (LEU) and hydroxypropyl-beta-cyclodextrin (CD)) on physicochemical stability and aerosolization performance is essential element prior designing the final dosage form. Stability tests (stress and accelerated) were performed at 40±2°C and 75±5% RH during 6 months. Particle characterization and size measurement - as the most important parameters in aerodynamic behavior - were done by the laser diffraction method, the surface morphology of microparticles was evaluated by scanning electron microscopy (SEM). The physiochemical properties of microparticles were investigated by X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC). The resulting aerodynamic behavior of microparticles was studied by Andersen cascade impactor. The overall stability results (against RH and temperature) showed that microparticles containing CIP and LEU alone and in combination with the other excipients were more stable than those containing PVA or CD alone. In relation to fine particle fraction and mass median aerodynamic diameter (determining the aerosolization parameters), it was found that the particle size and particle shape did not show significant changes after the storage. Among the excipients LEU was found to have many advantages, including relatively simple formulation, enhanced aerosolization behaviour, convenient portability and inherently improved stability. Such a composition may serve as an innovative drug delivery system for the local treatment of respiratory tract infection and cystic fibrosis.

Authors+Show Affiliations

Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Faculty of Pharmacy, Szeged, Hungary.Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Faculty of Pharmacy, Szeged, Hungary.Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Faculty of Pharmacy, Szeged, Hungary.Institute of Pharmaceutical Technology and Regulatory Affairs, University of Szeged, Faculty of Pharmacy, Szeged, Hungary. Electronic address: arita@pharm.u-szeged.hu.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

28965047

Citation

Karimi, Keyhaneh, et al. "Physicochemical Stability and Aerosolization Performance of Dry Powder Inhalation System Containing Ciprofloxacin Hydrochloride." Journal of Pharmaceutical and Biomedical Analysis, vol. 148, 2018, pp. 73-79.
Karimi K, Katona G, Csóka I, et al. Physicochemical stability and aerosolization performance of dry powder inhalation system containing ciprofloxacin hydrochloride. J Pharm Biomed Anal. 2018;148:73-79.
Karimi, K., Katona, G., Csóka, I., & Ambrus, R. (2018). Physicochemical stability and aerosolization performance of dry powder inhalation system containing ciprofloxacin hydrochloride. Journal of Pharmaceutical and Biomedical Analysis, 148, 73-79. https://doi.org/10.1016/j.jpba.2017.09.019
Karimi K, et al. Physicochemical Stability and Aerosolization Performance of Dry Powder Inhalation System Containing Ciprofloxacin Hydrochloride. J Pharm Biomed Anal. 2018 Jan 30;148:73-79. PubMed PMID: 28965047.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Physicochemical stability and aerosolization performance of dry powder inhalation system containing ciprofloxacin hydrochloride. AU - Karimi,Keyhaneh, AU - Katona,Gábor, AU - Csóka,Ildikó, AU - Ambrus,Rita, Y1 - 2017/09/22/ PY - 2017/04/28/received PY - 2017/09/11/revised PY - 2017/09/13/accepted PY - 2017/10/2/pubmed PY - 2018/7/4/medline PY - 2017/10/2/entrez KW - Aerodynamic behavior KW - Ciprofloxacin hydrochloride KW - Co-spray-drying KW - Dry powder inhalation KW - Microparticles KW - Stress and accelerated stability test SP - 73 EP - 79 JF - Journal of pharmaceutical and biomedical analysis JO - J Pharm Biomed Anal VL - 148 N2 - Antibiotic delivery in form of dry powder inhalation has been studied for possible clinical treatment of respiratory tract infection in the recent years. Dry powder inhalation of ciprofloxacin hydrochloride (CIP) assures local antibacterial activity and comfort of easy application. The aim of this work was to test the stability of co-spray-dried CIP in carrier free system. Since the microparticles in the dry powder system are amorphous and do not contain any stabilizer, the effects of temperature and relative humidity (RH) on the physicochemical properties and aerosolization behavior are very important. Therefore investigation of the role of excipients (such as polyvinyl alcohol (PVA), l-leucine (LEU) and hydroxypropyl-beta-cyclodextrin (CD)) on physicochemical stability and aerosolization performance is essential element prior designing the final dosage form. Stability tests (stress and accelerated) were performed at 40±2°C and 75±5% RH during 6 months. Particle characterization and size measurement - as the most important parameters in aerodynamic behavior - were done by the laser diffraction method, the surface morphology of microparticles was evaluated by scanning electron microscopy (SEM). The physiochemical properties of microparticles were investigated by X-ray powder diffraction (XRPD) and differential scanning calorimetry (DSC). The resulting aerodynamic behavior of microparticles was studied by Andersen cascade impactor. The overall stability results (against RH and temperature) showed that microparticles containing CIP and LEU alone and in combination with the other excipients were more stable than those containing PVA or CD alone. In relation to fine particle fraction and mass median aerodynamic diameter (determining the aerosolization parameters), it was found that the particle size and particle shape did not show significant changes after the storage. Among the excipients LEU was found to have many advantages, including relatively simple formulation, enhanced aerosolization behaviour, convenient portability and inherently improved stability. Such a composition may serve as an innovative drug delivery system for the local treatment of respiratory tract infection and cystic fibrosis. SN - 1873-264X UR - https://www.unboundmedicine.com/medline/citation/28965047/Physicochemical_stability_and_aerosolization_performance_of_dry_powder_inhalation_system_containing_ciprofloxacin_hydrochloride_ DB - PRIME DP - Unbound Medicine ER -