Nonlinear data fitting for controlled release devices: An integrated computer program
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Summary
A computer program, MSFIT, was developed for nonlinear fitting of release data from controlled release devices, written in the C language, based on the high level user-interface Macintosh operating system.
- Type
- article
- Published
- 1996-03-08
- Cited by
- 23
- References
- 19
- OpenAlex
- https://openalex.org/W1985280860
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:94418553
Keywords
Computer program, Nonlinear system, Curve fitting, Computer science, Interface (matter)
References
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- Applied regression analysis 2nd ed.
- Preparation and release kinetics of hydrochlorothiazide from butyl half-ester of PVM/MA microcapsules.
- Influence of additives on (hydroxyethyl) methylcellulose properties: relation between gelation temperature change, compressed matrix integrity and drug release profile
- An evaluation of albumin microcapsules prepared using a multiple emulsion technique.
- Progesterone-loaded albumin microparticles
- Numerical Recipes in C: The Art of Scientific Computing
- MECHANISM OF SUSTAINED-ACTION MEDICATION. THEORETICAL ANALYSIS OF RATE OF RELEASE OF SOLID DRUGS DISPERSED IN SOLID MATRICES.
- Ibuprofen-loaded ethylcellulose microspheres: release studies and analysis of the matrix structure through the Higuchi model.
- Analysis of Fickian and non-Fickian drug release from polymers.
- Controlled release: mechanisms and release.
- Applied Regression Analysis.
- Modeling of Pharmacokinetic Data
Cited by
- In vivo evaluation of zidovudine (AZT)-loaded ethylcellulose microspheres after oral administration in beagle dogs.
- Dissolution properties and anticonvulsant activity of phenytoin-polyethylene glycol 6000 and -polyvinylpyrrolidone K-30 solid dispersions.
- Drug dissolution profiles from polymeric matrices: Data versus numerical solution of the diffusion problem and kinetic models
- The use of FT-IR imaging as an analytical tool for the characterization of drug delivery systems.
- Magnetic Fe₃ O ₄ nanoparticles grafted with single-chain antibody (scFv) and docetaxel loaded β-cyclodextrin potential for ovarian cancer dual-targeting therapy.
- DDSolver: An Add-In Program for Modeling and Comparison of Drug Dissolution Profiles
- Facile synthesis of amphiphilic chitosan-g-poly(lactic acid) derivatives and the study of their controlled drug release
- Optima: a windows-based program for computer-aided optimization of controlled-release dosage forms.
- Comparison of dissolution profiles of Ibuprofen pellets.
- Physicochemical characterization and in vivo properties of Zolpidem in solid dispersions with polyethylene glycol 4000 and 6000.
- Mechanism of drug release from silicone microspheres containing Polycarbophil
- Complexation of phenytoin with some hydrophilic cyclodextrins: effect on aqueous solubility, dissolution rate, and anticonvulsant activity in mice.
- Optimization of propranolol hydrochloride sustained release pellets using a factorial design
- Optimization of propranolol hydrochloride sustained-release pellets using box-behnken design and desirability function.
- Modeling and comparison of dissolution profiles.
- Silicone microspheres for pH-controlled gastrointestinal drug delivery.
- PREPARATION OF NIOSOMES CONTAINING CHLORAMPHENICOL SODIUM SUCCINATE AND EVALUATION OF THEIR PHYSICOCHEMICAL AND ANTIMICROBIAL PROPERTIES
- Formulation and Evaluation of an Herbal Cream from Dry Extract of Glycyrrhiza Globra and Fumaria Parviflora
- Characterization of polymer blends as mucoadhesive materials for gastroretentive drug delivery system
- Vancomycin release kinetics from Mg–Ca silicate porous microspheres developed for controlled drug delivery
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