Automatic Dissolution Testing with High-Temporal Resolution for Both Immediate-Release and Fixed-Combination Drug Tablets

Dissolution testing plays many important roles throughout the pharmaceutical industry, from the research and development of drug products to the control and evaluation of drug quality. However, it is a challenging task to perform both high-efficient separation and high-temporal detection to achieve accurate dissolution profile of each active ingredient dissolved from a drug tablet. In our study, we report a novel non-manual-operation method for performing the automatic dissolution testing of drug tablets, by combining a program-controlled sequential analysis and high-speed capillary electrophoresis for efficient separation of active ingredients. The feasibility of the method for dissolution testing of real drug tablets as well as the performance of the proposed system has been demonstrated. The accuracy of drug dissolution testing is ensured by the excellent repeatability of the sequential analysis, as well as the similarity of the evaluation of dissolution testing. Our study show that the proposed method is capable to achieve simultaneous dissolution testing of multiple ingredients, and the matrix interferences can be avoided. Therefore it is of potential valuable applications in various fields of pharmaceutical research and drug regulation.

[1]  P. Costa,et al.  Modeling and comparison of dissolution profiles. , 2001, European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences.

[2]  C. Lehr,et al.  In Situ Drug Release Monitoring with a Fiber-Optic System: Overcoming Matrix Interferences Using Derivative Spectrophotometry , 2013 .

[3]  Vivian A. Gray,et al.  Power of the Dissolution Test in Distinguishing a Change in Dosage Form Critical Quality Attributes , 2018, AAPS PharmSciTech.

[4]  Andreas M. Abend,et al.  Industry's View on Using Quality Control, Biorelevant, and Clinically Relevant Dissolution Tests for Pharmaceutical Development, Registration, and Commercialization. , 2018, Journal of pharmaceutical sciences.

[5]  Yong Gan,et al.  Novel gastroretentive sustained-release tablet of tacrolimus based on self-microemulsifying mixture: in vitro evaluation and in vivo bioavailability test , 2011, Acta Pharmacologica Sinica.

[6]  Jesper ϕstergaard UV imaging in pharmaceutical analysis , 2018, Journal of pharmaceutical and biomedical analysis.

[7]  R. Mashru,et al.  Simultaneous determination of salbutamol sulphate, bromhexine hydrochloride and etofylline in pharmaceutical formulations with the use of four rapid derivative spectrophotometric methods. , 2007, Analytica chimica acta.

[8]  Thomas Rades,et al.  Biorelevant intrinsic dissolution profiling in early drug development: Fundamental, methodological, and industrial aspects. , 2019, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[9]  J. Martínez Calatayud,et al.  Automated simultaneous triple dissolution profiles of two drugs, sulphamethoxazole-trimethoprim and hydrochlorothiazide-captopril in solid oral dosage forms by a multicommutation flow-assembly and derivative spectrophotometry. , 2004, Journal of pharmaceutical and biomedical analysis.

[10]  N. Dovichi,et al.  Nicked-sleeve interface for two-dimensional capillary electrophoresis. , 2013, The Analyst.

[11]  Khan Ka,et al.  Effect of compaction pressure on the dissolution efficiency of some direct compression systems. , 1972 .

[12]  Xujin Lu,et al.  In Situ UV Fiber Optics for Dissolution Testing – What, Why, and Where We Are After 30 Years , 2018 .

[13]  Qingling Li,et al.  Consecutive Gated Injection-Based Microchip Electrophoresis for Simultaneous Quantitation of Superoxide Anion and Nitric Oxide in Single PC-12 Cells. , 2016, Analytical chemistry.

[14]  Q. Fang,et al.  A Low-Cost Palmtop High-Speed Capillary Electrophoresis Bioanalyzer with Laser Induced Fluorescence Detection , 2018, Scientific Reports.

[15]  Q. Fang,et al.  Improved high‐speed capillary electrophoresis system using a short capillary and picoliter‐scale translational spontaneous injection , 2014, Electrophoresis.

[16]  W. Schuhmann,et al.  Robotic microplate voltammetry for real-time hydrogel drug release testing. , 2018, Analytica chimica acta.

[17]  N. Petersen,et al.  UV-vis Imaging of Piroxicam Supersaturation, Precipitation, and Dissolution in a Flow-Through Setup. , 2018, Analytical chemistry.

[18]  Patrick Marroum,et al.  In Vivo Bioequivalence and In Vitro Similarity Factor (f2) for Dissolution Profile Comparisons of Extended Release Formulations: How and When Do They Match? , 2011, Pharmaceutical Research.

[19]  N. Fotaki,et al.  Surface Dissolution UV Imaging for Investigation of Dissolution of Poorly Soluble Drugs and Their Amorphous Formulation , 2019, AAPS PharmSciTech.

[20]  J. Dressman,et al.  Can dosage form-dependent food effects be predicted using biorelevant dissolution tests? Case example extended release nifedipine. , 2016, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

[21]  R. Marini,et al.  Validation of analytical methods involved in dissolution assays: acceptance limits and decision methodologies. , 2012, Analytica chimica acta.

[22]  S. Coombes,et al.  Proton NMR: a new tool for understanding dissolution. , 2014, Analytical chemistry.

[23]  P. Tůma,et al.  Hydrodynamic sample injection into short electrophoretic capillary in systems with a flow-gating interface. , 2017, Journal of chromatography. A.

[24]  J. Jorgenson,et al.  A Transparent Flow Gating Interface for the Coupling of Microcolumn LC with CZE in a Comprehensive Two-Dimensional System , 1993 .

[25]  Qiyang Zhang,et al.  Prototyping of poly(dimethylsiloxane) interfaces for flow gating, reagent mixing, and tubing connection in capillary electrophoresis. , 2014, Journal of chromatography. A.

[26]  F. Podczeck COMPARISON OF IN-VITRO DISSOLUTION PROFILES BY CALCULATING MEAN DISSOLUTION TIME (MDT) OR MEAN RESIDENCE TIME (MRT) , 1993 .

[27]  S. Ozkan,et al.  Simultaneous Determination and Drug Dissolution Testing of Combined Amlodipine Tablet Formulations Using RP-LC , 2016, Chromatographia.

[28]  B. V. Araújo,et al.  Development of a dissolution method based on lipase for preclinical level A IVIVC of oral poly(ε-caprolactone) microspheres , 2019, Journal of Drug Delivery Science and Technology.

[29]  J. Locs,et al.  Development of local strontium ranelate delivery systems and long term in vitro drug release studies in osteogenic medium , 2018, Scientific Reports.

[30]  Q. Fang,et al.  Automatic Combination of Microfluidic Nanoliter-Scale Droplet Array with High-Speed Capillary Electrophoresis , 2016, Scientific Reports.

[31]  L. Cabral,et al.  Development of a Dissolution Method for Gliclazide Modified-Release Tablets Using USP Apparatus 3 with in Vitro-in Vivo Correlation. , 2018, Chemical & pharmaceutical bulletin.

[32]  K. A. Khan,et al.  Further studies of the effect of compaction pressure on the dissolution efficiency of direct compression systems. , 1974, Pharmaceutica acta Helvetiae.

[33]  W. Weitschies,et al.  In‐vitro dissolution methods for controlled release parenterals and their applicability to drug‐eluting stent testing , 2012, The Journal of pharmacy and pharmacology.

[34]  M. K. Abd El-Rahman,et al.  UV-spectrophotometry versus HPLC–PDA for dual-drug dissolution profiling: which technique provides a closer step towards green biowaiver concept? Novel application on the recent FDA-approved mixture Aleve pm , 2018, Chemical Papers.

[35]  M. Steppe,et al.  Monolithic LC method applied to fesoterodine fumarate low dose extended-release tablets: Dissolution and release kinetics , 2014, Journal of pharmaceutical analysis.

[36]  R. Löbenberg,et al.  The Significance of disintegration testing in pharmaceutical development , 2018 .

[37]  Patrick J. Sinko,et al.  Martin's physical pharmacy and pharmaceutical sciences : physical chemical and biopharmaceutical principles in the pharmaceutical sciences , 2006 .

[38]  M. Bowser,et al.  High-Speed, Comprehensive, Two Dimensional Separations of Peptides and Small Molecule Biological Amines Using Capillary Electrophoresis Coupled with Micro Free Flow Electrophoresis. , 2017, Analytical chemistry.