Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Formulation development and evaluation of osmotic drug delivery system for lornoxicam

View through CrossRef
Osmotic systems are the most reliable controlled drug delivery systems and can be employed as oral drug delivery systems. Osmotic pressure is used as the driving force for these systems to release the drug in a controlled manner. Osmotic pump tablet (OPT) generally consists of a core including the drug(s), an osmotic agent, other excipients and semipermeable membrane coat. The aim of current study was to develop osmotic drug delivery system for Lornoxicam. Two different approaches were used for formulation, one was controlled porosity osmotic tablet and other was elementary osmotic tablet. The formulations were evaluated for different parameters like appearance, uniformity of weight, drug content, hardness and drug release also the effect of different osmotic agents responsible for developing the osmotic pressure such as sodium chloride and mannitol along with different concentration of pore former sorbitol were studied and comparison was made between first controlled porosity osmotic tablet which include the osmotic tablet in which coating membrane contains water soluble pore forming polymers when the membrane comes in contact with water the leaching of polymers occur thereby permitting the water inside the wall and creating the osmotic pressure to release the drug and second the elementary osmotic tablet containing osmotic agent sodium chloride coated with the rate controlling semipermeable membrane of cellulose acetate, this membrane contains an orifice of a critical size through which the drug is delivered. From the results it was found that the developed formulation the controlled porosity osmotic tablet of Lornoxicam (CPOP) was able to release the drug over 12 hrs at zero order and also the concentration of osmotic agent, level of pore former and thickness of coating membrane are responsible for controlling the release of Lornoxicam. The coating membrane was subjected to SEM analysis which showed formation of pores in the membrane. The developed controlled porosity osmotic pump tablet of lornoxicam was found to control the release for 12 hrs.
Title: Formulation development and evaluation of osmotic drug delivery system for lornoxicam
Description:
Osmotic systems are the most reliable controlled drug delivery systems and can be employed as oral drug delivery systems.
Osmotic pressure is used as the driving force for these systems to release the drug in a controlled manner.
Osmotic pump tablet (OPT) generally consists of a core including the drug(s), an osmotic agent, other excipients and semipermeable membrane coat.
The aim of current study was to develop osmotic drug delivery system for Lornoxicam.
Two different approaches were used for formulation, one was controlled porosity osmotic tablet and other was elementary osmotic tablet.
The formulations were evaluated for different parameters like appearance, uniformity of weight, drug content, hardness and drug release also the effect of different osmotic agents responsible for developing the osmotic pressure such as sodium chloride and mannitol along with different concentration of pore former sorbitol were studied and comparison was made between first controlled porosity osmotic tablet which include the osmotic tablet in which coating membrane contains water soluble pore forming polymers when the membrane comes in contact with water the leaching of polymers occur thereby permitting the water inside the wall and creating the osmotic pressure to release the drug and second the elementary osmotic tablet containing osmotic agent sodium chloride coated with the rate controlling semipermeable membrane of cellulose acetate, this membrane contains an orifice of a critical size through which the drug is delivered.
From the results it was found that the developed formulation the controlled porosity osmotic tablet of Lornoxicam (CPOP) was able to release the drug over 12 hrs at zero order and also the concentration of osmotic agent, level of pore former and thickness of coating membrane are responsible for controlling the release of Lornoxicam.
The coating membrane was subjected to SEM analysis which showed formation of pores in the membrane.
The developed controlled porosity osmotic pump tablet of lornoxicam was found to control the release for 12 hrs.

Related Results

Selection of Injectable Drug Product Composition using Machine Learning Models (Preprint)
Selection of Injectable Drug Product Composition using Machine Learning Models (Preprint)
BACKGROUND As of July 2020, a Web of Science search of “machine learning (ML)” nested within the search of “pharmacokinetics or pharmacodynamics” yielded over 100...
Overview on Osmotic Drug Delivery System
Overview on Osmotic Drug Delivery System
The aim of the current review is to elaborate on the osmotic drug delivery system for controlled release of drugs. The oral route is the most conventional and acceptable route of d...
Solubility enhancement of lornoxicam with poloxamer 188 by solvent evaporation method
Solubility enhancement of lornoxicam with poloxamer 188 by solvent evaporation method
This investigation aimed to enhance the solubility and bioavailability of the BCS class II poorly water-soluble drug Lornoxicam by solid dispersion (SD) techniques using Polaxomer ...
Efficacy of Lornoxicam as a Pre-emptive Analgesic in Mandibular Third Molar Surgery – A Comparative Study
Efficacy of Lornoxicam as a Pre-emptive Analgesic in Mandibular Third Molar Surgery – A Comparative Study
Abstract Introduction: The most common complication following third molar surgery is pain. The purpose of the study is to determine the efficacy ...
Non-Recommended Publishing Lists: Strategies for Detecting Deceitful Journals
Non-Recommended Publishing Lists: Strategies for Detecting Deceitful Journals
Abstract The rapid growth of open access publishing (OAP) has significantly improved the accessibility and dissemination of scientific knowledge. However, this expansion has also c...
Design and evaluation of lornoxicam bilayered tablets for biphasic release
Design and evaluation of lornoxicam bilayered tablets for biphasic release
The objective of the present investigation was to develop bilayered tablets of lornoxicam to achieve biphasic release pattern. A bilayered tablet, consisting of an immediate and co...
OSMOTIC AND PULSATILE DRUG DELIVERY SYSTEMS: ENGINEERING CHRONOTHERAPEUTIC PRECISION FOR CONTROLLED THERAPEUTIC OUTCOMES
OSMOTIC AND PULSATILE DRUG DELIVERY SYSTEMS: ENGINEERING CHRONOTHERAPEUTIC PRECISION FOR CONTROLLED THERAPEUTIC OUTCOMES
The technologies of controlled drug delivery have made an impact on therapeutic arena through optimizing the pharmacokinetic profile, improving patient adherence as well as reducin...
Development of Solid Self – Nanoemulsified Drug Delivery System Containing Rosuvastatin
Development of Solid Self – Nanoemulsified Drug Delivery System Containing Rosuvastatin
This study aims to solidify the self-nanoemulsifying drug delivery system with rosuvastatin (SNEDDS Ros) for application in solid dosage forms. The liquid SNEDDS Ros system is soli...

Back to Top