Identifying sources of error and variability in dissolution calibration and sample testing

American Pharmaceutical Review

Volumn 5, Issue 2, 2002, Pages 8-12

  Gray, Vivian A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

DRUG; PREDNISONE; SALICYLIC ACID;

ANALYTIC METHOD; ANALYTICAL ERROR; ARTICLE; CALIBRATION; CONTROLLED STUDY; DRUG FORMULATION; DRUG SCREENING; DRUG SOLUBILITY; LABORATORY APPARATUS, EQUIPMENT AND SUPPLIES; LABORATORY AUTOMATION; PH; SAMPLE; TABLET FORMULATION; TEMPERATURE; VIBRATION;

EID: 0036061632     PISSN: 10998012     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

1. Fine-Tuning of Dissolution Apparatus for the Apparatus Suitability Test Using the USP Dissolution Calibrators
2. Dissolution Calibrator: Recommendations for Reduced Chemical Testing and Enhanced Mechanical Calibration
3. Dissolution Testing: A Fast, Efficient Procedure for Degassing Dissolution Medium
4. Impact of Different Deaeration Methods on the USP Dissolution Apparatus Suitability Test Criteria
5. Vibration-What Is It and How Does It Affect Dissolution Testing
6. A Comparison of Dissolution Results using O-ring versus Clipped Basket Shafts"
7. Dissolution Method Development for Poorly Soluble Compounds
8. ANDA Dissolution Method Development and Validation
9. A New General Chapter on Dissolution
10. Dissolution Media for In Vitro Testing of Water-Insoluble drugs, Effect of Surfactant Purity and Electrolyte on In Vitro Dissolution of Carbamazepine in Aqueous Solutions of Sodium Lauryl Sulfate
11. Effects of Sinker Shapes on Dissolution Profiles