Abstract

A REVIEW: PHARMACEUTICAL SUSPENSION AND ITS ADVANCEMENT

Sneha L. Kewade, Pooja R. Hatwar*, Dr. R. L. Bakal, J. A. Kubde and R. M. Atram

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Abstract

Additionally, pharmaceutical suspension is classified based on the nature of drug particles, particle size, and method of preparation. Various factors such as viscosity, sedimentation rate, and redispersibility affect the stability of the suspension. The formulation of the suspension involves selection of appropriate excipients, surfactants, and stabilizers to enhance the solubility and stability of the drug particles. Packaging of suspension is also crucial to prevent physical and chemical instabilities during storage. Furthermore, the review emphasizes the importance of regulatory requirements for pharmaceutical suspension. Good manufacturing practices (GMP) and quality control procedures are necessary to ensure the safety, efficacy, and quality of these formulations. The regulatory authorities also provide guidelines for the characterization, testing, and labeling of pharmaceutical suspension. In conclusion, pharmaceutical suspension is a widely used dosage form due to its high bioavailability and ease of administration. The properties, formulation, stability, and regulatory requirements of suspension are crucial to ensure the safety and efficacy of the medication.

Keywords: Pharmaceutical suspension, Formulation of suspension, Preservation of suspension, Nanosuspension.