Different types, applications and limits of enabling excipients of pharmaceutical dosage forms.
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Summary
The purpose of this review is to provide an overview of different types of excipients in relation to their application possibilities in various dosage forms with special focus on the enablingexcipients.
- Type
- review
- Published
- 2018-07-01
- Cited by
- 9
- References
- 136
- OpenAlex
- https://openalex.org/W2802285071
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:51973631
Keywords
Dosage form, Biochemical engineering, Excipient, Computer science, Pharmaceutical sciences
References
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- The Influence of Surfactant HLB and Oil/Surfactant Ratio on the Formation and Properties of Self-emulsifying Pellets and Microemulsion Reconstitution
- Solid self-nanoemulsifying drug delivery system (S-SNEDDS) of darunavir for improved dissolution and oral bioavailability: In vitro and in vivo evaluation.
- Physical stability of API/polymer‐blend amorphous solid dispersions
- The effect of commonly used vehicles on canine hematology and clinical chemistry values.
- Development and Optimization of Solid Self Nanoemulsifying Drug Delivery (S-SNEDDS) Using D-Optimal Design for Improvement of Oral Bioavailability of Amiodarone Hydrochloride.
- Simvastatin nanolipid carriers decreased hypercholesterolemia induced cholesterol inclusion and phosphatidylserine exposure on human erythrocytes
- Effect of hydroxypropylcellulose and Tween 80 on physicochemical properties and bioavailability of ezetimibe-loaded solid dispersion.
- A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability
- Effect of bile on the oral absorption of halofantrine in polyethylene glycol 400 and polysorbate 80 formulations dosed to bile duct cannulated rats
- Nanocrystal technology, drug delivery and clinical applications
- Handbook of Lipid Bilayers
- Effect of drug physico-chemical properties on the efficiency of top-down process and characterization of nanosuspension
- Effect of particle size on solubility, dissolution rate, and oral bioavailability: evaluation using coenzyme Q10 as naked nanocrystals
- Using Flory–Huggins phase diagrams as a pre‐formulation tool for the production of amorphous solid dispersions: a comparison between hot‐melt extrusion and spray drying
- Stability and Solubility of Celecoxib-PVP Amorphous Dispersions: A Molecular Perspective
- A comparative solubility enhancement profile of valdecoxib with different solubilization approaches
- Effect of temperature, cosolvent, and added drug on Pluronic-flurbiprofen micellization.
Cited by
- Quality by Design Based Formulation Study of Meloxicam-Loaded Polymeric Micelles for Intranasal Administration
- Interaction of Commonly Used Oral Molecular Excipients with P-glycoprotein
- Microbes, Clinical trials, Drug Discovery, and Vaccine Development: The Current Perspectives
- Another Move towards Bicalutamide Dissolution and Permeability Improvement with Acetylated β-Cyclodextrin Solid Dispersion
- Functionality-related characteristics of hydroxypropyl-β-cyclodextrin for the complexation
- The practice of dividing tablets: An uncertain act
- Introduction in thermoplastic and thermosetting polymers
- REVIEW ON HYDROTROPY: A POTENTIAL APPROACH FOR THE SOLUBILITY ENHANCEMENT OF POORLY SOLUBLE DRUG
- Degradation versus resorption
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