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Nanosuspension: An approach to enhance solubility of drugs

Open access
Agrawal, YK, Patel, VishalR·2011·Journal of Advanced Pharmaceutical Technology & Research

Abstract

One of the major problems associated with poorly soluble drugs is very low bioavailability. The problem is even more complex for drugs like itraconazole, simvastatin, and carbamazepine which are poorly soluble in both aqueous and nonaqueous media, belonging to BCS class II as classified by biopharmaceutical classification system. Formulation as nanosuspension is an attractive and promising alternative to solve these problems. Nanosuspension consists of the pure poorly water-soluble drug without any matrix material suspended in dispersion. Preparation of nanosuspension is simple and applicable to all drugs which are water insoluble. A nanosuspension not only solves the problems of poor solubility and bioavailability, but also alters the pharmacokinetics of drug and thus improves drug safety and efficacy. This review article describes the preparation methods, characterization, and applications of the nanosuspension.

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Metadata

Authors
Agrawal, Y., & Patel, V.
Venue
Journal of Advanced Pharmaceutical Technology & Research
Publisher
Medknow
Published
2011
Volume
2
Issue
2
Pages
81
ISSN
  • 0976-2094 (ISSN-L)
  • 2231-4040
OpenAlex
W2103037903
Cited by
682
References
0
FWCI
5.21
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Nanosuspension: An approach to enhance solubility of drugs. https://app.cochat.ai/papers/10.4103/2231-4040.82950
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Agrawal, Y., & Patel, V. (2011). Nanosuspension: An approach to enhance solubility of drugs. Journal of Advanced Pharmaceutical Technology & Research. https://doi.org/10.4103/2231-4040.82950

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.