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IJSDR
INTERNATIONAL JOURNAL OF SCIENTIFIC DEVELOPMENT AND RESEARCH
International Peer Reviewed & Refereed Journals, Open Access Journal
ISSN Approved Journal No: 2455-2631 | Impact factor: 8.15 | ESTD Year: 2016
open access , Peer-reviewed, and Refereed Journals, Impact factor 8.15

Issue: May 2024

Volume 9 | Issue 5

Impact factor: 8.15

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Paper Title: AN OVERVIEW OF NANOSUSPENSION PREPARATION, CHARACTERIZATION, AND EVALUATION AS A STRATEGY FOR POORLY SOLUBLE DRUGS
Authors Name: Lavkush Santosh Jadhav , Dr. Avinash H. Hosmani , Poonam B. Mane , Divyani D. Mane , Vishnu V. Mali
Unique Id: IJSDR2401037
Published In: Volume 9 Issue 1, January-2024
Abstract: Abstract :- The speed at which the drug development process is progressing is producing a number of novel drug candidates with good therapeutic efficacy but poor water solubility. Because of its unique physicochemical characteristics and submicron particle size, nanosuspension holds the potential to address numerous formulation and drug delivery challenges that are commonly linked to poorly soluble medicines in water and fat. To manufacture and scale-up nanosuspensions, conventional size reduction tools like media mills and high-pressure homogenizers as well as formulation strategies including solvent diffusion, emulsion-solvent evaporation, precipitation, and microemulsion procedures can be effectively used. For the successful manufacture and scaling-up of nanosuspensions, it is important to take into account two crucial factors: maintaining the stability in both the solid and solution states and resuspendability without aggregation. The versatility for surface modification and mucoadhesion for drug targeting, along with the notable improvement in bioavailability, have greatly broadened the application of this innovative formulation approach. Much research is now being done on the use of nanosuspensions in various drug delivery methods, including oral, ophthalmic, brain, topical, buccal, nasal, and transdermal routes. Receptor-mediated endocytosis in combination with oral drug delivery in nanosuspension has great promise for resolving most permeability-limited absorption and hepatic first-pass metabolism-related problems that negatively impact bioavailability. The development of enabling technologies, including nanosuspension, can address numerous formulation issues that currently plague protein and as well as peptide based formulation.
Keywords: Nanosuspension, novel drug delivery, solubility enhancement, Surfactant.
Cite Article: "AN OVERVIEW OF NANOSUSPENSION PREPARATION, CHARACTERIZATION, AND EVALUATION AS A STRATEGY FOR POORLY SOLUBLE DRUGS", International Journal of Science & Engineering Development Research (www.ijsdr.org), ISSN:2455-2631, Vol.9, Issue 1, page no.267 - 276, January-2024, Available :http://www.ijsdr.org/papers/IJSDR2401037.pdf
Downloads: 000338719
Publication Details: Published Paper ID: IJSDR2401037
Registration ID:209806
Published In: Volume 9 Issue 1, January-2024
DOI (Digital Object Identifier):
Page No: 267 - 276
Publisher: IJSDR | www.ijsdr.org
ISSN Number: 2455-2631

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