Literature DB >> 14727896

Novel mathematical method for quantitative expression of deviation from the higuchi model.

M C Gohel1, M K Panchal, V V Jogani.   

Abstract

A simple mathematical method to express the deviation in release profile of a test product following Higuchi's kinetics from an ideal Higuchi release profile was developed. The method is based on calculation of area under the curve (AUC) by using the trapezoidal rule. The precision of prediction depends on the number of data points. The method is exemplified for 2 dosage forms (tablets of diltiazem HCl and microspheres of diclofenac sodium) that are designed to release the drug over a 12-hour period. The method can be adopted for the formulations where drug release is incomplete (<100%) or complete (100%) at last sampling time. To describe the kinetics of drug release from the test formulation, zero-order, first-order, Higuchi's, Hixson-Crowell's, and Weibull's models were used. The criterion for selecting the most appropriate model was based on the goodness-of-fit test. The release kinetics of the tablets and microspheres were explained by the Higuchi model. The release profiles of the test batches were slightly below the ideal Higuchi release profile. For the test products, observed percentage deviation from an ideal Higuchi profile is less than 16% for tablets and less than 11% for microspheres. The proposed method can be extended to the modified release formulations that are designed to release a drug over 6, 18, or 24 hours. If the data points are not evenly separated, the ideal drug release profile and AUC are calculated according to the specific sampling time. The proposed method may be used for comparing formulated products during the research and development stage, for quality control of the products, or for promoting products by comparing performance of the test product with that of the innovator's product.

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Year:  2000        PMID: 14727896      PMCID: PMC2750455          DOI: 10.1208/pt010431

Source DB:  PubMed          Journal:  AAPS PharmSciTech        ISSN: 1530-9932            Impact factor:   3.246


  6 in total

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Authors:  T HIGUCHI
Journal:  J Pharm Sci       Date:  1963-12       Impact factor: 3.534

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Authors:  T HIGUCHI
Journal:  J Pharm Sci       Date:  1961-10       Impact factor: 3.534

3.  An exponential expression for in vitro release of drug from sustained-release preparations.

Authors:  R G WIEGAND; J D TAYLOR
Journal:  Drug Stand       Date:  1959 Nov-Dec

4.  Relationship between swelling, erosion and drug release in hydrophillic natural gum mini-matrix formulations.

Authors:  J Sujja-areevath; D L Munday; P J Cox; K A Khan
Journal:  Eur J Pharm Sci       Date:  1998-07       Impact factor: 4.384

5.  Square root of time dependence of matrix formulations with low drug content.

Authors:  H Fessi; J P Marty; F Puisieux; J T Carstensen
Journal:  J Pharm Sci       Date:  1982-07       Impact factor: 3.534

6.  Formulation optimization of controlled release diclofenac sodium microspheres using factorial design.

Authors:  M C Gohel; A F Amin
Journal:  J Control Release       Date:  1998-02-12       Impact factor: 9.776

  6 in total
  5 in total

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Authors:  John Mark Christensen; Monica Chang Chuong; Hang Le; Loan Pham; Ehab Bendas
Journal:  Arch Drug Inf       Date:  2011-03

2.  Formulation, Pharmacokinetic, and Efficacy Studies of Mannosylated Self-Emulsifying Solid Dispersions of Noscapine.

Authors:  Terrick Andey; Apurva Patel; Srujan Marepally; Mahavir Chougule; Shawn D Spencer; Arun K Rishi; Mandip Singh
Journal:  PLoS One       Date:  2016-01-12       Impact factor: 3.240

3.  Effects of Compositional Tailoring on Drug Delivery Behaviours of Silica Xerogel/Polymer Core-shell Composite Nanoparticles.

Authors:  Wenfei Huang; Chi Pong Tsui; Chak Yin Tang; Linxia Gu
Journal:  Sci Rep       Date:  2018-08-29       Impact factor: 4.379

4.  Development of Perphenazine-Loaded Solid Lipid Nanoparticles: Statistical Optimization and Cytotoxicity Studies.

Authors:  Parisa Abbasi Farsani; Reza Mahjub; Mojdeh Mohammadi; Seyed Sajad Oliaei; Mohammad Mehdi Mahboobian
Journal:  Biomed Res Int       Date:  2021-04-28       Impact factor: 3.411

5.  Solid lipid nanoparticles of a water soluble drug, ciprofloxacin hydrochloride.

Authors:  M Shah; Y K Agrawal; K Garala; A Ramkishan
Journal:  Indian J Pharm Sci       Date:  2012-09       Impact factor: 0.975

  5 in total

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