Solubility and Partition Coefficient of Salicylamide in Various pH Buffer Solutions
Dewi Isadiartuti(1*), Noorma Rosita(2), Esti Hendradi(3), Firdausiah Fania Dwi Putri Putri(4), Frida Magdalena(5)
(1) Department of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C Mulyorejo, Surabaya 60115, Indonesia
(2) Department of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C Mulyorejo, Surabaya 60115, Indonesia
(3) Department of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C Mulyorejo, Surabaya 60115, Indonesia
(4) Department of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C Mulyorejo, Surabaya 60115, Indonesia
(5) Department of Pharmaceutical Sciences, Faculty of Pharmacy, Universitas Airlangga, Campus C Mulyorejo, Surabaya 60115, Indonesia
(*) Corresponding Author
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[1] Hughes, J.P., Rees, S., Kalindjian, S.B., and Philpott, K.L., 2011, Principles of early drug discovery, Br. J. Pharmacol., 162 (6), 1239–1249.
[2] National Center for Biotechnology Information, 2020, PubChem Compound Summary for CID 5147, Salicyl amide, https://pubchem.ncbi.nlm.nih.gov/compound/ Salicylamide, accessed on 15 December 2020.
[3] Rizk, M., and Abdel-Rahman, M.S., 1994, Salicylamide reverses the aspirin-antagonistic effect of salicylic acid on rat platelet cyclooxygenase, Prostaglandins, Leukotrienes Essent. Fatty Acids, 51 (5), 363–367.
[4] Brayfield, A., 2014, Martindale: The Complete Drug Reference, 38th Ed., Pharmaceutical Press (PhP), London.
[5] Shargel, L., and Yu, A.B.C., 2016, Applied Biopharmaceutics and Pharmacokinetics, 7th Ed., Mc Graw-Hill Education, New York, 263–264, 425–437.
[6] Xiao, C., Zhu, L., Li, R., Pang, L., Zhu, S., Ma, J., Du, L., and Jin, Y., 2020, Electroporation-enhanced transdermal drug delivery: Effects of log P, pKa, solubility, and penetration time, Eur. J. Pharm. Sci., 151, 105410.
[7] Zhang, Q., Wang, Z., Xue, H., Huang, B., Lin, Z., and Cai, Z., 2021, Determination and comparison of the solubility, oil-water partition coefficient, intestinal absorption, and biliary excretion of carvedilol enantiomers, AAPS PharmSciTech, 22 (1), 43.
[8] Plöger, G.F., Hofsäss, M.A., and Dressman, J.B., 2018, Solubility determination of active pharmaceutical ingredients which have been recently added to the list of essential medicines in the context of the biopharmaceutics classification system-biowaiver, J. Pharm. Sci., 107 (6), 1478–1488.
[9] Isadiartuti, D., Budiati, T., and Martodihardjo, S., 2015, Bioavailability study of physical mixture of carbamazepine and amino acid, Asian J. Pharm. Clin. Res., 8 (3), 92–95.
[10] Pobudkowska, A., and Domańska, U., 2014, Study of pH dependent drugs solubility in water, Chem. Ind. Chem. Eng., 20 (1), 115–126.
[11] Hamed, R., Awadallah, A., Sunoqrot, S., Tarawneh, O., Nazzal, S., AlBaraghthi, T., Al Sayyad, J., and Abbas, A., 2016, pH-Dependent solubility and dissolution behavior of carvedilol-Case example a weakly basic BCS class II drug, AAPS PharmSciTech, 17 (2), 418–426.
[12] Loh, Z.H., Samanta, A.K., and Heng, P.W.S., 2015, Overview of milling techniques for improving the solubility of poorly water-soluble drugs, Asian J. Pharm. Sci., 10 (4), 255–274.
[13] Sharma, T., and Jana, S., 2020, Investigation of molecular properties that influence the permeability and oral bioavailability of major β‑boswellic acids, Eur. J. Drug Metab. Pharmacokinet., 45 (2), 243–255.
[14] Nugrahaeni, F., Hariyadi, D.M., and Rosita, N., 2018, Partition coefficient and glutathione penetration of topical antiaging: Preformulation study, Int. J. Drug. Delivery Technol., 8 (2), 39–43.
[15] Rosita, N, Meitasari, V.A., Rianti, M.C., Hariyadi, D.M., and Miatmoko, A., 2019, Enhancing skin penetration of epigallocatechin gallate by modifying partition coefficient using reverse micelle method, Ther. Delivery, 10 (7), 409–417.
[16] Czyrski, A., 2019, Determination of the liphophilicity of ibuprofen, naproxen, ketoprofen, and flurbiprofen with thin-layer chromatography, J. Chem., 2019, 3407091.
[17] Li, W., Quan, P., Zhang, Y., Cheng, J., Liu, J., Cun, D., Xiang, R., and Fang, L., 2014, Influence of drug physicochemical properties on absorption of water insoluble drug nanosuspensions, Int. J. Pharm., 460 (1-2), 13–23.
[18] Blake-Taylor, B.H., Deleon, V.H., Acree, W., and Abraham, M.H., 2007, Mathematical correlation of salicylamide solubilities in organic solvents with the Abraham solvation parameter model, Phys. Chem. Liq., 45 (4), 389–398.
[19] Laube, F., Klein, T., and Sadowski, G., 2015, Partition coefficient of pharmaceuticals as functions of temperatures and pH, Ind. Eng. Chem. Res., 54 (15), 3968–3975.
[20] Medić-Sarić, M., Mornar, A., and Jasprica, X., 2004, Lipophilicity study of salicylamide, Acta. Pharm., 54 (2), 91–101.
[21] Pavia, D.L., Lampman, G.M., Kriz, G.S., and Vyvyan, J.R., 2015, Introduction to Spectroscopy, 5th Ed., Cengage Learning, Washington, 29–30.
[22] Helmenstine, A.M., 2019, Bronsted Lowry Theory of Acids and Bases, https://thoughtco.com/bronsted-lowry-theory-of-acids-and-bases-4127201, accessed on Aug. 27, 2020.
[23] Vepuri, S.B., Anbazhagan, S., Divya, D., and Padmini, D., 2013, A review on supramolecular chemistry in drug design and formulation research, Indones. J. Pharm., 24 (3), 131–150.
[24] Hibbert, F., and Sellens, R.J., 1988, Intramolecular participation by an amide group in ester hydrolysis, J. Chem. Soc. Perkin Trans., 2 (3), 399–402.
DOI: https://doi.org/10.22146/ijc.66411
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