Development of HPLC Method for Stress Testing of Combination of Two Drugs Using Design of Experiment Concept
Abstract
This study was conducted to develop, an High Performance Liquid Chromatography using photodiode array detector (HPLC-PDA) method to analyse the samples generated by the stress testing of antifilarial combination (albendazole and diethylcarbamazine citrate) in the solution state. The concept of Quality by Design (Design of Experiment, DoE) approach was used for the development. For the separation of the drugs and its degradation products (DPs), DoE was applied in two stages, i.e., primary parameter stage where factors having major effect were selected. This stage gives us CQA (Critical Quality Attribute) which along with minor factors affecting were varied to get the secondary design. For each of the stage a different design was selected; for primary stage IV optimal design (Response Surface Method) was selected whereas for secondary stage, Taguchi orthogonal array design was selected. The major primary parameters affecting the HPLC method as screened by preliminary studies were the buffer pH, organic modifier (methanol or acetonitrile), initial hold time (start of gradient) and gradient time. The primary stage was completed successfully. The results were compiled in form of resolution of peak from next peak and analysed by DoE. The process fixed the values for buffer pH (4.38), organic modifier (acetonitrile) and gradient time (30 min). The CQA from primary run was initial hold time. This parameter along with other parameters: initial and final concentration of organic modifier, buffer type (phosphate or acetate), buffer strength (mM) and oven temperature were further varied and samples withdrawn were analysed. The data of secondary design was compiled in the form of resolution (R), analysed by Design Expert and final value for secondary parameter for HPLC method were fixed. The resolution of the peaks for some secondary runs was sufficient reflecting some type of interaction between the drugs and/or degradation products.
Keywords:
Albendazole, diethylcarbamazine, solution-state stability, HPLC, stress testing.DOI
https://doi.org/10.25004/IJPSDR.2019.110611References
World Health Organisation. First WHO report on neglected tropical diseases. Geneva, 2010.
Lemk TL. Antiparasitic Agent. In: Thomas L. Lemke, editor. Foye's Principles of Medicinal Chemistry. Seventh ed. USA: Lippincott Williams & Wilkins; 2008. p. 1146-50.
Department of Control of Neglected Tropical Diseases (NTD). Preventive chemotherapy in human helminthiasis: coordinated use of anthelminthic drugs in control interventions: a manual for health professionals and programme managers. Geneva: 2006.
World Health Organisation. Alternating mass drug administration regimens to eliminate lymphatic filariasis. Geneva, 2017, p. 1-47.
Council of Europe. European Pharmacopoeia. Ninth ed. Strasbourg: Council of Europe; 2016. p. 1657-8.
Council of Europe. European Pharmacopoeia. Ninth ed. Strasbourg: Council of Europe; 2016. p. 2254-5.
International Conference on Harmonisation. Stability Testing of New Drug Substances and Products Q1A(R2), (2003).
Maheswaran R. FDA Perspectives: Scientific Considerations of Forced Degradation Studies in ANDA Submissions. Pharmaceutical Technology. 2012; 36(5):73-80.
Chakole RD, Charde MS, Kumar J, Welankiwar AS. Development of forced degradation studies of drugs. International Journal of Advances in Pharmaceutics. 2013; 2(3): 34-39.
Singh S, Bakshi M. Stress test to determine inherent stability of drugs. Pharm Technol. 2000; 4:1-14.
Klick S, Pim GM, Waterval J, et al. Toward a Generic Approach for Stress Testing of Drug Substances and Drug Products. Pharm Technol. 2005; 29(2):48-66.
Alsante KM, Martin L, Baertschi SW. A Stress Testing Benchmarking Study. Pharmaceutical Technology. 2003; 27(2): 60-72.
Sonawane S, Gide P. An experimental design approach for the forced degradation studies and development of a stability-indicating LC method for eplerenone in tablets. J Liq Chromatogr Relat Technol. 2011; 34:2020-2031.
Singh S, Modhe G, Tiwari H, Kurmi M, Parashar N, Sidduri P. Forced degradation studies to assess the stability of drugs and products. Trends Anal Chem. 2013; 49:71-88.
Sonawane S, Gide P. Optimization of forced degradation using experimental design and development of a stability-indicating liquid chromatographic assay method for rebamipide in bulk and tablet dosage form. Sci Pharm 2011; 79(1): 85-96.
Raijada DK, Prasad B, Paudel A, Shah RP, Singh S. Characterization of degradation products of amorphous and polymorphic forms of clopidogrel bisulphate under solid state stress conditions. J Pharm Biomed Anal. 2010; 52(3):332-44.
Kurmi M, Kumar S, Singh B, Singh S. Implementation of design of experiments for optimization of forced degradation conditions and development of a stability-indicating method for furosemide. Journal of Pharmaceutical and Biomedical Analysis. 2014; 96:135-43.
Dan W. Reynolds BKJ. Stresss testing of combination therapies. In: Baertschi SW, Alsante KM, Reed RA, editor. Pharmaceutical Stress Testing: Predicting Drug Degradation. Second ed. London: Informa Health; 2011. p. 448-55.
Kurmi M, Golla VM, Kumar S, Sahu A, Singh S. Stability behaviour of antiretroviral drugs and their combinations. 1: characterization of tenofovir disoproxil fumarate degradation products by mass spectrometry. RSC Advances. 2015; 5(116):96117-29.
Snyder LR, Kirkland JJ, Glajch JL. Practical HPLC Method Development. Second ed. USA: John Wiley & Sons; 1997.
Shah P, Patel J, Patel K, Gandhi T. Development and validation of an HPTLC method for the simultaneous estimation of clonazepam and paroxetine hydrochloride using a DOE approach. J Taibah Uni Sci. 2017; 11:121-32.
Bajaj M, Nanda S. Analytical quality by design (AQbD): new paradigm for analytical method development. Int J Dev Res. 2015; 5:3289-599.
Gholve SB, Ajgunde RR, Bhusnure OG, Thonte SS. Analytical method development and validation by QbD approach - a review. Der Pharmacia Sinica. 2015; 6:18-24.
Beg S, Sharma G, Katare OP, Shikha L, Singh B. Development and validation of a stability indicating liquid chromatographic method for estimating olmesartan medoxomil using quality by design. J Chromatogr Sci. 2015; 53:1048-59.
Kumar L Reddy MS, Managuli RS, Pai KG. Full factorial design for optimization, development and validation of HPLC method to determine valsartan in nanoparticles. Saudi Pharm J. 2015; 23:549- 55.
Food and Drug Administration International Conference on Harmonisation. Guidance on Q11 Development and Manufacture of Drug Substances; availability. Notice. Fed. Regist. 2012; 77:69634–69635.
N Politis S, Colombo P, Colombo G, M Rekkas D. Design of experiments (DoE) in pharmaceutical development. Drug Development and Industrial Pharmacy 2017; 43(6):889–901.
Abelson J, Simon M. Biothiols Part A Monothiols and Dithiols, Protein Thiols, and Thiyl Radicals. Academic Press, 1995.
Ullmann's Encyclopedia of Industrial Chemistry. 7 ed. Germany: Wiley‐VCH Verlag GmbH & Co, 2005.
Published

