Literature DB >> 34239296

Superhydrophobic Surface for Enhancing the Bioavailability of Salbutamol Sulfate from Cross-Linked Microspheres: Formulation, Characterization, and in vivo Evaluation.

Dalia Gaber1, Siham Abdoun1, Ameerah Alfuraihy2, Bushra Altasan2, Amal Alsubaiyel1.   

Abstract

INTRODUCTION: The aim of the work was to formulate salbutamol sulfate (SB) microspheres by using superhydrophobic surface (SHS) under different processing factors for improving its encapsulation efficiency, controling its release rate, and hence enhancing its bioavailability.
METHODS: Cross-linked microspheres of chitosan (CN) and carrageenan (KN) were made on a SHS under a glutaraldehyde-saturated atmosphere. The formulations were designed and optimized based on 42 factorial design. Percentage encapsulation efficiency (%EE), particle size, swelling ratio, and in vitro release rate were characterized, and the in vivo performance of optimized formula was investigated in beagle dogs.
RESULTS: The results showed that the prepared microspheres have a high %EE (97.11±0.78%) for F13. The swelling ratio was 4.2 at the end of the 8 hours for the optimized formula, and the in vitro release rate was controlled for 12 hours. In vivo study verified that there was a 1.61-fold enhancement in SB bioavailability from optimized formula (F13) compared to market tablet.
CONCLUSION: The study suggested that microspheres prepared from CN/KN crosslinking on an SHS using glutaraldehyde atmosphere is a promising technique that can encapsulate and sustain the release of water-soluble drugs such as SB in addition to improving its in vivo pharmacokinetic profile.
© 2021 Gaber et al.

Entities:  

Keywords:  bioavailability; cross-linked complex; microspheres; salbutamol sulfate; superhydrophobic; sustain release; water-soluble drugs

Mesh:

Substances:

Year:  2021        PMID: 34239296      PMCID: PMC8259835          DOI: 10.2147/DDDT.S309078

Source DB:  PubMed          Journal:  Drug Des Devel Ther        ISSN: 1177-8881            Impact factor:   4.162


  27 in total

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Authors:  Zhiguang Guo; Weimin Liu; Bao-Lian Su
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Review 5.  Mathematical modeling of drug dissolution.

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Journal:  Int J Pharm       Date:  2013-04-22       Impact factor: 5.875

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Journal:  Drug Deliv       Date:  2007-11       Impact factor: 6.419

7.  Formulation of ciprofloxacin hydrochloride loaded biodegradable nanoparticles: optimization of technique and process variables.

Authors:  Doaa H Mobarak; Salwa Salah; Seham A Elkheshen
Journal:  Pharm Dev Technol       Date:  2013-09-13       Impact factor: 3.133

8.  Preparation and evaluation of chitosan/carrageenan beads for controlled release of sodium diclofenac.

Authors:  Pimwipha Piyakulawat; Nalena Praphairaksit; Nuanphun Chantarasiri; Nongnuj Muangsin
Journal:  AAPS PharmSciTech       Date:  2007-11-16       Impact factor: 3.246

9.  A high bioavailability and sustained-release nano-delivery system for nintedanib based on electrospray technology.

Authors:  Hongfei Liu; Kunyu Du; Dongli Li; Yi Du; Jumei Xi; Ying Xu; Yan Shen; Tao Jiang; Thomas J Webster
Journal:  Int J Nanomedicine       Date:  2018-12-10
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