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Formulation Development and Characterization of Nanosuspension

AUTHOR Jivani, Rishad; Mohapatra, Dillip Kumar; Sahu, Asit Ranjan
PUBLISHER LAP Lambert Academic Publishing (09/04/2019)
PRODUCT TYPE Paperback (Paperback)

Description
This study was to identify and optimize formulation and process variables affecting characteristic and scale-up of nanosuspension manufacturing process on bead mill i.e media milling buttom down technique considering industrial perspective. Formulation factors evaluated were ratio of different polymer to drug and to beads. Whereas process parameters were milling bead concentration and stabilizer concentration. Responses measured in this study include zeta potential and mean particle size. The test revealed that ratio of polymer to drug have significant effect on zeta potential whereas variable milling bead concentration at constant milling speed and milling time have significant effect on the particle size distribution of nanosuspension. The X-ray powder diffraction pattern of drug milled at high and low speed reveals no form conversion when compared with unmilled drug. The formulated nanosuspension has shown a faster % cumulative release.
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Product Details
ISBN-13: 9786200306562
ISBN-10: 6200306567
Binding: Paperback or Softback (Trade Paperback (Us))
Content Language: English
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Page Count: 88
Carton Quantity: 80
Product Dimensions: 6.00 x 0.21 x 9.00 inches
Weight: 0.31 pound(s)
Country of Origin: US
Subject Information
BISAC Categories
Medical | Pharmacology
Descriptions, Reviews, Etc.
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This study was to identify and optimize formulation and process variables affecting characteristic and scale-up of nanosuspension manufacturing process on bead mill i.e media milling buttom down technique considering industrial perspective. Formulation factors evaluated were ratio of different polymer to drug and to beads. Whereas process parameters were milling bead concentration and stabilizer concentration. Responses measured in this study include zeta potential and mean particle size. The test revealed that ratio of polymer to drug have significant effect on zeta potential whereas variable milling bead concentration at constant milling speed and milling time have significant effect on the particle size distribution of nanosuspension. The X-ray powder diffraction pattern of drug milled at high and low speed reveals no form conversion when compared with unmilled drug. The formulated nanosuspension has shown a faster % cumulative release.
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