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Relevant bibliographies by topics / Solubility of HCl

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Journal articles

Academic literature on the topic 'Solubility of HCl'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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Journal articles on the topic "Solubility of HCl"

1

Copur, Mehmet, Sabri Colak, and Sinan Yapici. "Solubility of stibnite ore in HCl solutions." Industrial & Engineering Chemistry Research 34, no. 11 (1995): 3995–4002. http://dx.doi.org/10.1021/ie00038a040.

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2

Williams, Leah R., and David M. Golden. "Solubility of HCL in sulfuric acid at stratospheric temperatures." Geophysical Research Letters 20, no. 20 (1993): 2227–30. http://dx.doi.org/10.1029/93gl02607.

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3

Dominé, Florent, Emmanuel Thibert, Frank Van Landeghem, Eric Silvente, and Patrick Wagnon. "Diffusion and solubility of HCl in ice: preliminary results." Geophysical Research Letters 21, no. 7 (1994): 601–4. http://dx.doi.org/10.1029/94gl00512.

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4

Prakash, K., P. Narayana Raju, K. Shanta Kumari, and M. Lakshmi Narasu. "Solubility and Dissolution Rate Determination of Different Antiretroviral Drugs in Different pH Media Using UV Visible Spectrophotometer." E-Journal of Chemistry 5, s2 (2008): 1159–64. http://dx.doi.org/10.1155/2008/125917.

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Solubility and dissolution rate of three antiretroviral drugs such as lamivudine, zidovudine and stavudine was studied in four media having different pH. The samples were analyzed by usingUVVisible spectrophotometer. lamivudine shows more solubility that is 276.08 mg/mL in 0.01 N HCl. Stavudine showing highest solubility that is 101.23 mg/mL in pH 4.5 acetate buffer. Zidovudine showing highest solubility that is 28.90 mg/mL in both water and 0.01 N HCl. All three drugs showing lower solubility in pH 6.8 phosphate buffer. Lamivudine and stavudine showing good dissolution rate in all media and s

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5

Li, Yahong, Pengsheng Song, Shuping Xia, Wu Li, and Shiyang Gao. "Solubility prediction for the HCl–MgCl2–H2O system at 40 ∘C and solubility equilibrium constant calculation for HCl ⋅ MgCl2 ⋅ 7H2O at 40 ∘C." Calphad 30, no. 1 (2006): 61–64. http://dx.doi.org/10.1016/j.calphad.2005.10.008.

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6

Skiba, G. S., Yu A. Bezymyanova, and N. B. Voskoboinikov. "Solubility in the systems AlCl3-SrCl2-HCl-H2O and NaCl-SrCl2-HCl-H2O at 25°C." Russian Journal of Inorganic Chemistry 52, no. 9 (2007): 1464–67. http://dx.doi.org/10.1134/s0036023607090264.

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7

Mittal, Ankit, Manish Yadav, Dinesh Choudhary, and Birendra Shrivastava. "ENHANCEMENT OF SOLUBILITY OF LURASIDONE HCL USING SOLID DISPERSION TECHNIQUE." International Journal of Research in Ayurveda & Pharmacy 5, no. 5 (2014): 632–37. http://dx.doi.org/10.7897/2277-4343.055129.

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8

Fein, Jeremy B., and John V. Walther. "Calcite solubility and speciation in supercritical NaCl-HCl aqueous fluids." Contributions to Mineralogy and Petrology 103, no. 3 (1989): 317–24. http://dx.doi.org/10.1007/bf00402918.

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9

Darusman, Fitrianti, Taufik Muhammad Fakih, and Gina Fuji Nurfarida. "Identification of the Glimepiride and Metformin Hydrochloride Physical Interaction in Binary Systems." Borneo Journal of Pharmacy 4, no. 2 (2021): 110–16. http://dx.doi.org/10.33084/bjop.v4i2.1826.

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Glimepiride is often combined with metformin HCl as an oral antidiabetic in type II diabetes mellitus, which provides a complementary and synergistic effect with multiple targets for insulin secretion. Glimepiride includes class II of BCS, which solubility practically insoluble in water but high permeability, which will impact the drug's small bioavailability. In contrast, metformin HCl includes class III of BCS, which has a high solubility in water, but low permeability is absorbed approximately 50-60% in the digestive tract given orally. The co-crystallization method can be used to improve t

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10

Kumar, S. Sudalai, Ranjit Thakuria, and Ashwini Nangia. "Pharmaceutical cocrystals and a nitrate salt of voriconazole." CrystEngComm 16, no. 22 (2014): 4722–31. http://dx.doi.org/10.1039/c3ce42324g.

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Novel crystalline forms of voriconazole are identified with improved aqueous solubility. The dinitrate salt of voriconazole exhibited 10 fold higher solubility and 3 times faster dissolution rate in 0.1 N HCl medium compared to the reference drug.

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