Research & Reviews: A Journal of Drug Design & Discovery Article

Distinctive Approaches for Improving the Aqueous Solubility of BCS Class II Drugs

  1. Panner Selvam R Department of Pharmaceutics, T. John College of Pharmacy, Bengaluru
  2. Ganesh N.S Department of Pharmaceutics, T. John College of Pharmacy, Bengaluru
  3. Prince Shukla Department of Pharmaceutical Chemistry, T. John College of Pharmacy, Bengaluru
  4. Vineeth Chandy r, Department of Pharmaceutical Chemistry, T. John College of Pharmacy, Bengaluru

Abstract

The most difficult feature of many novel chemical entities is their solubility behaviour, as 60 percent of new promising products suffer solubility limitations. This is the most common reason for novel medicine compounds failing to reach the market or performing to their full potential. The proportion of the aqueous phase when the solution is in equilibrium with the pure substance in its normal phase is referred to as aqueous solubility. The greatest dose strength of an immediate release medication is used to determine solubility. Physical and chemical alteration of the medication, as well as other strategies, has all been used to boost the solubility of poorly soluble drugs. The pharmacological qualities, absorption site, and desired dosage form characteristics all influence which solubility augmentation strategy is used. This review article examines various novel ways to improving the solubility of weakly water-soluble compounds.

Keywords

References (53)

  1. Surawase RK, Baheti1 BG, Maru AD. Solubility enhancement techniques for poorly water-
  2. soluble drugs: a review. Eur J Bio Pharma Sci. 2020; 7(9): 124-36p.
  3. Patel V, Patel R, Shah H, Purohit S, Pawar M, Pathan A. Solubility enhancement of azithromycin
  4. by solid dispersion technique using Mannitol and β-Cyclodextrin. Acta Sci PharmaSci. 2021;
  5. 5(4): 48-54p.
  6. Jagtap S, Magdum C, Jadge D, Jagtap R. Solubility Enhancement Technique: A Review. J Pharm
  7. Sci & Res. 2018; 10(9): 2205-11p.
  8. R Lobenberg, GL Amidon. Modern bioavailability, bioequivalence and biopharmaceutics
  9. classification system. New scientific approaches to international regulatory standards. Eur J
  10. Pharma Biopharma. 2000; 50(1): 3-12p.
  11. Fouad SA, Malaak FA, El-Nabarawi MA, Zeid KA, Ghoneim AM. Preparation of solid dispersion
  12. systems for enhanced dissolution of poorly water soluble diacerein: In-vitro evaluation,
  13. optimization and physiologically based pharmacokinetic modeling. 2021; 16(1): 1-14p.
  14. Sanjaymitra PVSS, Ganesh GNK. Dissolution and solubility enhancement strategies: current and
  15. novel prospective. J Crit Rev. 2018; 5(3): 1-10p.
  16. Gupta R, Jain V, Nagar JC, Ansari A, Sharma K, Sarkar A, Khan MS. Bioavailability
  17. enhancement techniques for poorly soluble drugs: a review. Asian J Pharma Res Dev. 2020; 8(2):
  18. Alshehria S, Imama SS, Hussaina A. Potential of solid dispersions to enhance solubility,
  19. bioavailability, and therapeutic efficacy of poorly water-soluble drugs: newer formulation
  20. techniques, current marketed scenario and patents. Drug delivery. 2020; 27(1): 1625-43p
  21. Huang S, Williams RO. Effects of process on the properties of amorphous solid dispersions.
  22. AAPS PharmSciTech. 2018; 19(5): 1971-84p.
  23. Tan K, DavisJr DA, Miller DA, Williams III RO, Nokhodchi A. Innovations in thermal
  24. processing: hot-melt extrusion and kinetisol® dispersing deck. AAPS PharmSciTech. 2020;
  25. 21(312): 1-20p
  26. Crowley MM, Zhang F, Repka MA, Thumma S, Upadhye SB, Kumar Battu S. Pharmaceutical
  27. applications of hot-melt extrusion: part I. Drug Dev Ind Pharm. 2007; 33(9): 909-26p.
  28. Li X, Anton N, Arpagaus C, Belleteix F, Vandamme TF. Nanoparticles by spray drying using
  29. new innovative technology: The Buchi nano spray dryer B 90. J Control Release. 2010; 147(2):
  30. Tripathi R, Biradar SV, Mishra B, Paradkar AR. Study of polymorphs of progesterone by novel
  31. melt sonocrystallization technique: A technical note. AAPS Pharm Sci Tech. 2010; 11(3): 1493-
  32. Bala R, Madaan R, Arora S. Advanced solubility enhancement techniques for poorly soluble
  33. drugs. J Pharma Sci Tech. 2017; 7(1): 6-11p.
  34. Adali MB, Barresi AA, Boccardo G, Pisano R. Spray freeze-drying as a solution to continuous
  35. manufacturing of pharmaceutical products in bulk. Processes. 2020; 8(709): 1-27p.
  36. Radke R, Jain NK. Melt sonocrystallization a novel technique of solubility enhancement: a
  37. review. Int J Pharm Sci Rev Res. 2020; 64(2): 70-75p.
  38. Sopan P, Nilesh M, Purushottam G, Amol W. Enhancement of solubility of diclofenac sodium by
  39. pastillation method. J Drug Deli & Therap. 2021; 11(2): 6-10p.
  40. Pandit. PA, Chavan TT, Khandelwal RK. Oral lipid based multipurticulate pastilles: Design and
  41. effect of pore former. J Pharma Invest. 2015; 45: 1-9p.
  42. Thakur V, Dogra1 S, Verma S, Vashist HR. Solubility enhancement techniques. World J Pharma
  43. Res. 2020; 9(13): 265-82p.
  44. Gaddam M, Ravouru N. A Crystal engineering design to enhance the solubility, dissolution,
  45. stability and micromeritic properties of omeprazole via co-crystallization techniques. Research J.
  46. Pharm. and Tech. 2021; 14(1): 356-62p.
  47. Patel JN, Rathod DM, Patel NA, Modasiya MK. Techniques to improve the solubility of poorly
  48. soluble drugs. Int J Pharm & Life Sci. 2012; 3(2): 1459-69p.
  49. Kumar RS, Sai JD. Liquisolid Compacts: A Review. J Drug Delivery & Thera. 2019; 9(4): 880-
  50. Xing H, Jiang J, Chen X, Yang T, Wang D, Ding P. Liquisolid technique and its applications in
  51. pharmaceutics. Asian J Pharma Sci 2017; 12(2): 115-23p
  52. Savkare AD, Bhavsar MR, Gholap VD, Kukkar PM. Liquisolid technique: a review. Int J Pharma
  53. Sci Res 2017; 8(7): 2768-75p.
Support