Novel in-situ gel for intravesical administration of ketorolac

The urinary bladder stores urine until the time of urination. Systemic administration of drugs to treat bladder diseases faces several limitations. Therefore, intravesical drug delivery is a promising alternative route of administration. An in-situ gel is used to form a gel inside the bladder cavity...

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Main Authors: Abdelrahman Y. Sherif, Gamal Mohamed Mahrous, Fars Kaed Alanazi
Format: Article
Language:English
Published: Elsevier 2018-09-01
Series:Saudi Pharmaceutical Journal
Online Access:http://www.sciencedirect.com/science/article/pii/S131901641830077X
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spelling doaj-95be18b870f7426eae9cdc57d3b0c4552020-11-24T22:36:36ZengElsevierSaudi Pharmaceutical Journal1319-01642018-09-01266845851Novel in-situ gel for intravesical administration of ketorolacAbdelrahman Y. Sherif0Gamal Mohamed Mahrous1Fars Kaed Alanazi2Kayyali Chair for Pharmaceutical Industries, Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi ArabiaCorresponding author at: Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh 11454, P.O. Box 2457, Saudi Arabia.; Kayyali Chair for Pharmaceutical Industries, Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi ArabiaKayyali Chair for Pharmaceutical Industries, Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi ArabiaThe urinary bladder stores urine until the time of urination. Systemic administration of drugs to treat bladder diseases faces several limitations. Therefore, intravesical drug delivery is a promising alternative route of administration. An in-situ gel is used to form a gel inside the bladder cavity and ensure continuous release of the drug even after urination. The objective of the present study was to optimize an in-situ gel formulation of poloxamer and chitosan for intravesical delivery of ketorolac tromethamine. The gelling temperature of the prepared combinations ranged from 20.67 to 25.8 °C. In-vitro release of KT was sustained for up to 7 h using a poloxamer concentration ranging from 17% to 19% and a chitosan concentration ranging from 1% to 2%. Design-Expert® 10 was used to select the optimized formulation (poloxamer/chitosan 17/1.589% w/w) which significantly (p < 0.05) extended the drug release more than each polymer alone. An ex-vivo study showed the ability of the optimized formulation to sustain drug release after emptying two times to mimic urination. Furthermore, the formed gel adhered to the bladder tissue throughout the time period of the experiment. Intravesical administration of the optimized formulation to rabbits via catheter showed no obstruction of urine flow and continuous release of the drug for 12 h. Keywords: Intravesical, In-situ gel, Ketorolac, Poloxamer 407, Chitosanhttp://www.sciencedirect.com/science/article/pii/S131901641830077X
collection DOAJ
language English
format Article
sources DOAJ
author Abdelrahman Y. Sherif
Gamal Mohamed Mahrous
Fars Kaed Alanazi
spellingShingle Abdelrahman Y. Sherif
Gamal Mohamed Mahrous
Fars Kaed Alanazi
Novel in-situ gel for intravesical administration of ketorolac
Saudi Pharmaceutical Journal
author_facet Abdelrahman Y. Sherif
Gamal Mohamed Mahrous
Fars Kaed Alanazi
author_sort Abdelrahman Y. Sherif
title Novel in-situ gel for intravesical administration of ketorolac
title_short Novel in-situ gel for intravesical administration of ketorolac
title_full Novel in-situ gel for intravesical administration of ketorolac
title_fullStr Novel in-situ gel for intravesical administration of ketorolac
title_full_unstemmed Novel in-situ gel for intravesical administration of ketorolac
title_sort novel in-situ gel for intravesical administration of ketorolac
publisher Elsevier
series Saudi Pharmaceutical Journal
issn 1319-0164
publishDate 2018-09-01
description The urinary bladder stores urine until the time of urination. Systemic administration of drugs to treat bladder diseases faces several limitations. Therefore, intravesical drug delivery is a promising alternative route of administration. An in-situ gel is used to form a gel inside the bladder cavity and ensure continuous release of the drug even after urination. The objective of the present study was to optimize an in-situ gel formulation of poloxamer and chitosan for intravesical delivery of ketorolac tromethamine. The gelling temperature of the prepared combinations ranged from 20.67 to 25.8 °C. In-vitro release of KT was sustained for up to 7 h using a poloxamer concentration ranging from 17% to 19% and a chitosan concentration ranging from 1% to 2%. Design-Expert® 10 was used to select the optimized formulation (poloxamer/chitosan 17/1.589% w/w) which significantly (p < 0.05) extended the drug release more than each polymer alone. An ex-vivo study showed the ability of the optimized formulation to sustain drug release after emptying two times to mimic urination. Furthermore, the formed gel adhered to the bladder tissue throughout the time period of the experiment. Intravesical administration of the optimized formulation to rabbits via catheter showed no obstruction of urine flow and continuous release of the drug for 12 h. Keywords: Intravesical, In-situ gel, Ketorolac, Poloxamer 407, Chitosan
url http://www.sciencedirect.com/science/article/pii/S131901641830077X
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