Jug et al., 2017 - Google Patents
In vitro dissolution/release methods for mucosal delivery systemsJug et al., 2017
View PDF- Document ID
- 13399091584472673459
- Author
- Jug M
- Hafner A
- Lovrić J
- Lusina Kregar M
- Pepić I
- Vanić
- Cetina-Čižmek B
- Filipović-Grčić J
- Publication year
- Publication venue
- ADMET and DMPK
External Links
Snippet
Sažetak In vitro dissolution/release tests are an indispensable tool in the drug product development, its quality control and the regulatory approval process. Mucosal drug delivery systems are designed to provide both local and systemic drug action following ocular, nasal …
- 238000004090 dissolution 0 title abstract description 44
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay
- G01N33/543—Immunoassay; Biospecific binding assay with an insoluble carrier for immobilising immunochemicals
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N1/00—Sampling; Preparing specimens for investigation
- G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
- G01N1/40—Concentrating samples
- G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/5005—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving human or animal cells
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N13/00—Investigating surface or boundary effects, e.g. wetting power; Investigating diffusion effects; Analysing materials by determining surface, boundary, or diffusion effects
- G01N2013/003—Diffusion; diffusivity between liquids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N13/00—Investigating surface or boundary effects, e.g. wetting power; Investigating diffusion effects; Analysing materials by determining surface, boundary, or diffusion effects
- G01N2013/006—Dissolution of tablets or the like
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Olejnik et al. | Active compounds release from semisolid dosage forms | |
| US20100089186A1 (en) | Device for evaluation of pharmaceutical compositions | |
| Jug et al. | In vitro dissolution/release methods for mucosal delivery systems | |
| US10228358B2 (en) | Apparatus and method for the assessment of concentration profiling and permeability rates | |
| Kregar et al. | Development and validation of an in vitro release method for topical particulate delivery systems | |
| Beyssac et al. | Dissolution study of active pharmaceutical ingredients using the flow through apparatus USP 4 | |
| JP5608282B2 (en) | Polymer membrane with human skin-like permeability and use thereof | |
| US8652087B2 (en) | Method for use of microdialysis | |
| CN110736813A (en) | Method for measuring in-vitro release rate of pharmaceutical preparations | |
| JP2006505802A (en) | Raised surface assay plate | |
| US11185827B2 (en) | Modified filter membrane and the use thereof | |
| Vrhovec et al. | A microfluidic diffusion chamber for reversible environmental changes around flaccid lipid vesicles | |
| CA2495521A1 (en) | Methods of measuring the dissolution rates of an analyte in a non-aqueous liquid composition | |
| Jeong et al. | Revisiting in vitro release test for topical gel formulations: The effect of osmotic pressure explored for better bio-relevance | |
| Fecioru et al. | In vitro performance testing of nanoparticulate drug products for parenteral administration | |
| Jain et al. | An Artificial Gut/Absorption Simulator: Understanding the Impact of Absorption on In Vitro Dissolution, Speciation, and Precipitation of Amorphous Solid Dispersions | |
| CN103822978A (en) | Method for measuring related substances in entecavir tablets by liquid chromatography | |
| US20210096120A1 (en) | Method for determining release rates of active principle ingredients from at least one semisolid form | |
| Hiew et al. | In Vitro Dissolution of Pharmaceutical Solids | |
| CN106461514B (en) | Media for blood sample collection and transport | |
| Barnett | Controlled release of oxaminiquine from polymer films | |
| Shinde et al. | A REVIEW ON DISSOLUTION TEST APPARATUS WITH THEIR DIFFERENT MODEL | |
| Sutthapitaksakul et al. | Effect of processing parameters on release profiles of donepezil hydrochloride-loaded microparticles | |
| Roper | Role of insulin signaling in pancreatic beta cells and measurement of insulin release from islets of Langerhans using a microfluidic chip | |
| Shah | Characterization of free dissolved drug concentrations in vitro using pulsatile microdialysis: Application to supersaturation and drug distribution |