Effect of moisture on solid state stability
DOI:
https://doi.org/10.20883/medical.e908Keywords:
water-solid interactions, physico-chemical changes of solids, drug products stability, drug products bioavaiabilityAbstract
Water is omnipresent during pharmaceutical product manufacturing and may interact with the drug substance, excipients, and the drug product in either solvent or vapor form, resulting in several physico-chemical changes, ultimately affecting product performance. Therefore, understanding the mechanisms behind such moisture-induced changes is necessary at every stage of pharmaceutical development and manufacturing to obtain the target formulation.
Characterization tools, such as water sorption, spectroscopy, thermal analysis, diffraction, and more sophisticated approaches like simulations and PAT techniques, can help in the selection of the appropriate solid form, manufacturing method, excipients, and storage conditions, enabling the manufacturing of a stable drug product formulation.
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References
Paroma Chakravarty, Karthik Nagapudi, The importance of water-solid interactions in small molecule drug development: An industry perspective, Trends in Analytical Chemistry 140 (2021) 116276. DOI: https://doi.org/10.1016/j.trac.2021.116276
G. Zografi, States of water associated with solids, Drug Dev. Ind. Pharm. 14 (1988) 1905-1926.
A.S. Narang, D. Desai, S. Badawy, Impact of Excipient Interactions on SolidDosage Form Stability, Pharmaceutical Research, 29 (2012) 2660-2683, DOI :10.1007/s11095-012-0782-9.
J.W. Collier, R.B. Shah, A. Gupta, V. Sayeed, M.J. Habib, M.A. Khan, Influence of formulation and processing factors on stability of levothyroxine sodium pentahydrate, AAPS PharmSciTech 11 (2010) 818.825.
R. Teraoka, M. Otsuka, Y. Matsuda, Effects of temperature and relative humidityon the solid-state chemical stability of ranitidine hydrochloride,J. Pharmaceut. Sci. 82 (1993) 601-604.
N.K. Patel, I.J. Patel, A.J. Cutie, D.A. Wadke, D.C. Monkhouse, G.E. Reier, The effect of selected direct compression excipients on the stability of aspirin as a model hydrolyzable drug, Drug Dev. Ind. Pharm. 14 (1988) 77-98
H. Morrison, B.P. Quan, S.D. Walker, K.B. Hansen, K. Nagapudi, S. Cui, Appearance of a new hydrated form during development: a case study in process and solid-state optimization, Org. Process Res. Dev. 19(12) (2015), 1842–1848 DOI:10.1021/acs.oprd.5b00030
S. Debnath, R. Suryanarayanan, Influence of processing-induced phase transformations on the dissolution of theophylline tablets, AAPS PharmSciTech 5 2004) 39-49.
Mehak Mehta,Khushboo Kothari , et al. Effect of Water on Molecular Mobility and Physical Stability of Amorphous Pharmaceuticals, Mol. Pharmaceutics 13, 4, ( 2016), 1339–1346, https://doi.org/10.1021/acs.molpharmaceut.5b00950
David A. Hirsh, Yongchao Su et al., Quantifying Disproportionation in Pharmaceutical Formulations with 35Cl Solid-State NMR, Mol. Pharmaceutics 15, 9, (2018) 4038–4048, https://doi.org/10.1021/acs.molpharmaceut.8b00470.
Haichen Nie, Gerard Klinzing, Wei Xu, A comparative study of applying backscattering and transmission Raman spectroscopy to quantify solid-state form conversion in pharmaceutical tablets, Int. J. Pharmaceutics, 617, 5 (2022), 121608, https://doi.org/10.1016/j.ijpharm.2022.121608.
B.R. Rohrs, T.J. Thamann, P. Gao, D.J. Stelzer, M.S. Bergren, R.S. Chao, Tablet dissolution affected by a moisture mediated solid-state interaction between drug and disintegrant, Pharmaceut. Res. 16 (1999) 1850-1856.
R. Steendam, H.W. Frijlink, C.F. Lerk, Plasticisation of amylodextrin by moisture. Consequences for compaction behaviour and tablet properties, Eur. J. Pharmaceut. Sci. 14 (2001) 245-254.
S. Fitzpatrick, J.F. McCabe, C.R. Petts, S.W. Booth, Effect of moisture on polyvinylpyrrolidone in accelerated stability testing, Int. J. Pharm. 246 (2002), 143-151.
Baladi, G.Y.; Rohani, B. Soil plasticity. In Theoretical Foundation for Large-Scale Computations for Nonlinear Material Behavior. Mechanics of Elastic and Inelastic Solids 6; Nemat-Nasser, S., Asaro, R.J., Hegemier, G.A., Eds.; Springer: Dordrecht, The Netherlands, 6, (1984); pp. 317–352, DOI: 10.1007/978-94-009-6213-2.
Komlan Koumbogle, Ryan Gosselin et al., Moisture Behavior of Pharmaceutical Powder during the Tableting Process, Pharmaceutics 15, (2023), 1652, https://doi.org/10.3390/pharmaceutics15061652.
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Accepted 2023-09-19
Published 2023-09-29