1. M. Yazdanian, K. Briggs, C. Jankovsky and A. Hawi, The »high solubility« definition of the current FDA Guidance on Biopharmaceutical Classification System may be too strict for acidic drugs, Pharm. Res. 21 (2004) 293-299; DOI: 10.1023/B:PHAM.0000016242.48642.71.10.1023/B:PHAM.0000016242.48642.71
2. L. X. Yu, G. L. Amidon, J. E. Polli, H. Zhao, M. U. Mehta, D. P. Conner, V. P. Shah, L. J. Lesko, M. Chen, V. H. L. Lee and A. S. Hussain, Biopharmaceutics classification system: The scientific basis for biowaiver extensions, Pharm. Res. 19 (2002) 921-925; DOI: 10.1023/A:1016473601633.10.1023/A:1016473601633
3. A. V. Yadav, A. S. Shete and A. P. Dabke, Formulation and evaluation of orodispersible liquisolid compacts of aceclofenac, Ind. J. Pharm. Educ. 44 (2010) 227-235.
4. Y. Javadzadeh, M. R. Siahi, S. Asnaashari and A. Nokhodchi, Liquisolid technique as a tool for enhancement of poorly water-soluble drugs and evaluation of their physicochemical properties, Acta Pharm. 57 (2007) 99-109; DOI: 10.2478/v10007-007-0008-6.10.2478/v10007-007-0008-6
5. S. Nazzal and M. A. Khan, Controlled release of a self-emulsifying formulation from a tablet dosage form: Stability assessment and optimization of some processing parameters, Int. J. Pharm. 315 (2006) 110-121; DOI: 10.1016/j.ijpharm.2006.02.019.10.1016/j.ijpharm.2006.02.019
6. N. Rasenack and B. W. Müller, Dissolution rate enhancement by in situ micronization of poorly water-soluble drugs, Pharm. Res. 19 (2002) 1894-1900; DOI: 10.1023/A:1021410028371.10.1023/A:1021410028371
7. A. B. Nighute and S. B. Bhise, Enhancement of dissolution rate of Rifabutin by preparation of microcrystals using solvent change method, Int. J. Pharm. Tech. Res. 1 (2009) 142-148.
8. G. V. Betager and K. R. Makarla, Enhancement of dissolution of glyburide by solid dispersion and lyophilization techniques, Int. J. Pharm. 126 (1995) 155-160; DOI: 10.1016/0378-5173(95) 04114-1.
9. J. W. Millard, F. A. Alvarez-Núñez and S. H. Yalkowsky Solubilization by cosolvents establishing useful constants for the log-linear model, Int. J. Pharm. 245 (2002) 153-166; DOI: 10.1016/ S0378-5173(02)00334-4.10.1016/S0378-5173(02)00334-4
10. P. Balakrishnan, B. Le, D. H. Oh, J. O. Kim, M. J. Hong, J. Jee, J. A. Kim, B. K. Yoo, J. S. Woo, C. S. Yong and H. Choi, Enhanced oral bioavailability of dexibuprofen by a novel solid self-emulsifying drug delivery system (SEDDS), Eur. J. Pharm. Biopharm. 72 (2009) 539-545; DOI: 10.1016/j. ejpb.2009.03.001.
11. A. Zvonar, K. Berginc, A. Kristl and M. Ga{perlin, Microencapsulation of self-microemulsifying system: Improving solubility and permeability of furosemide, Int. J. Pharm. 388 (2010) 151-158; DOI: 10.1016/j.ijpharm.2009.12.055.10.1016/j.ijpharm.2009.12.055
12. H. A. Hassan, A. H. Al-Marzouqi, B. Jobe, A. A. Hamza and G. A. Ramadan, Enhancement of dissolution amount and in vivo bioavailability of itraconazole by complexation with b-cyclodextrin using supercritical carbon dioxide, J. Pharmaceut. Biomed. 45 (2007) 243-250; DOI: 10.1016/j.jpba.2007.06.011.10.1016/j.jpba.2007.06.011
13. T. Tanino, T. Ogiso, M. Iwaki, G. Tanabe and O. Muraoka, Enhancement of oral bioavailability of phenytoin by esterification, and in vitro hydrolytic characteristics of prodrugs, Int. J. Pharm. 163 (1998) 91-102; DOI: 10.1016/S0378-5173(97)00374-8.10.1016/S0378-5173(97)00374-8
14. S. G. Kapsi and J. W. Ayres, Processing factors in development of solid solution formulation of itraconazole for enhancement of drug dissolution and bioavailability, Int. J. Pharm. 229(2001) 193-203; DOI: 10.1016/S0378-5173(01)00867-5.10.1016/S0378-5173(01)00867-5
15. D. X. Li, Y. Oh, S. Lim, J. O. Kim, H. J. Yang, J. H. Sung, C. S. Yong and H. Choi, Novel gelatin microcapsule with bioavailability enhancement of ibuprofen using spray-drying technique, Int.J. Pharm. 355 (2008) 277-284; DOI: 10.1016/j.ijpharm.2007.12.020.10.1016/j.ijpharm.2007.12.020
16. V. Stella, J. Haslam, N. Yata, H. Okada, S. Lindenbaum and T. Higuchi, Enhancement of bioavailability of a hydrophobic amine antimalarial by formulation with oleic acid in a soft gelatin capsule, J. Pharm. Sci. 67 (1978) 1375-1377.10.1002/jps.2600671011
17. V. K. Nagabandi, T. Ramarao and K. N. Jayaveera, Liquisolid compacts: A novel approach to enhance bioavailability of poorly soluble drugs, Int. J. Pharm. Biol. Sci. 1 (2011) 89-102.
19. K. Kavitha, K. N. S. LovaRaju, N. S. Ganesh and B. Ramesh, Effect of dissolution rate by liquisolid compacts approach: An overview, Der Pharmacia Lettre 3 (2011) 71-83.
21. S. M. Gavali, S. S. Pacharane, S. V. Sankpal, K. R. Jadhav and V. J. Kadam, Liquisolid compact: A new technique for enhancement of drug dissolution, Int. J. Res. Pharm. Chem. 1 (2011) 705-713.
22. A. B. Karmarkar, I. D. Gonjari, A. H. Hosmani, P. N. Dhabale and S. B. Bhise, Liquisolid tablets: A novel approach for drug delivery, Int. J. Health Res. 2 (2009) 45-50.
23. A. B. Karmarkar, I. D. Gonjari and A. H. Hosmani, Liquisolid technology for dissolution rate enhancement or sustained release, Expert Opin. Drug Deliv. 7 (2010) 1227-1234; DOI: 10.1517/17425247.2010.511173.10.1517/17425247.2010.511173
24. M. El-Hammadi and N. Awad, Investigating the use of liquisolid compacts technique to minimize the influence of pH variations on loratadine release, AAPSPharmSciTech. 13 (2012) 53-58; DOI: 10.1208/s12249-011-9719-6.10.1208/s12249-011-9719-6
25. A. K. Elkhodairy and M. W. Samy, Optimization and evaluation of micromeritic and release properties of high dose flutamide liquisolid systems, Lett. Drug Des. Discov. 9 (2012) 336-344; DOI: 10.2174/157018012799129873.10.2174/157018012799129873
26. Y. Javadzadeh, B. Jafari-Navimipour and A. Nokhodchi, Liquisolid technique for dissolution rate enhancement of a high dose water-insoluble drug (carbamazepine), Int. J. Pharm. 341 (2007) 26-34; DOI: 10.1016/j.ijpharm.2007.03.034.10.1016/j.ijpharm.2007.03.034
27. S. K. Singh, K. K. Srinivasan, K. Gowthamarajan, D. Prakash, N. B. Gaikwad and D. S. Singare, Influence of formulation parameters on dissolution rate enhancement of glyburide using liquisolid technique, Drug Dev. Ind. Pharm. 38 (2012) 961-970; DOI: 10.3109/03639045.2011.634810.10.3109/03639045.2011.634810
28. C. M. Hentzschel, A. Sakmann and C. S. Leopold, Suitability of various excipients as carrier and coating materials for liquisolid compacts, Drug Dev. Ind. Pharm. 37 (2011) 1200-1207; DOI: 10.3109/03639045.2011.564184.10.3109/03639045.2011.564184
29. B. M. El-Houssieny, L. F. Wahman and N. M. Arafa, Bioavailability and biological activity of liquisolid compact formula of repaglinide and its effect on glucose tolerance in rabbits, Biosci.Trends. 4 (2010) 17-24.
31. B. Chen, Z. Wang, G. Quan, X. Peng, X. Pan, R. Wang, Y. XU, G. Li and C. Wu, In vitro and in vivo evaluation of ordered mesoporous silica as a novel adsorbent in liquisolid formulation, Int. J. Nanomed. 7 (2012) 199-209; DOI: 10.2147/IJN.S26763.10.2147/IJN.S26763
32. R. H. Fahmy and M. A. Kassem, Enhancement of famotidine dissolution rate through liquisolid tablets formulation: In vitro and in vivo evaluation, Eur. J. Pharm. Biopharm. 69(2008) 993-1003; DOI: 10.1016/j.ejpb.2008.02.017.10.1016/j.ejpb.2008.02.017
33. I. D. Gonjari, A. B. Karmarkar and A. H. Hosmani, Evaluation of in vitro dissolution profile comparison methods of sustained release tramadol hydrochloride liquisolid compact formulations with marketed sustained release tablets, Dig. J. Nanomater. Bios. 4 (2009) 651-661.
34. H. S. Mahajan, M. R. Dhamne, S. G. Gattani, A. D. Rasal and H. T. Shaikh, Enhanced dissolution rate of glipizide by a liquisolid technique, Int. J. Pharm. Sci. Nanotech. 3 (2011) 1205-1213.
35. Y. Javadzadeh, L. Musaalrezaei and A. Nokhodchi, Liquisolid technique as a new approach to sustain propranolol hydrochloride release from tablet matrices, Int. J. Pharm. 362 (2008) 102-108; DOI: 10.1016/j.ijpharm.2008.06.022.10.1016/j.ijpharm.2008.06.022
36. A. Nokhodchi, R. Aliakbar, S. Desai and Y. Javadzadeh, Liquisolid compacts: The effect of cosolvent and HPMC in theophylline release, Colloid Surface B. 79 (2010) 262-269; DOI: 10.1016/j. colsurfb.2010.04.008.
37. Center for the Evaluation of Risks to Human Reproduction, NTP-CERHR Expert Panel report on the reproductive and developmental toxicity of propylene glycol, Reprod. Toxicol. 18 (2004) 533-579; DOI: 10.1016/j.reprotox.2004.01.004.10.1016/j.reprotox.2004.01.004
39. S. Gubbi and R. Jarag, Liquisolid Technique for enhancement of dissolution properties of bromhexine hydrochloride, Res. J. Pharm. Tech. 2 (2009) 382-386.
40. BASF group, Lutrol® E Liquid Grades, 2010; http://www.pharma-ingredients.basf.com/Statements/Technical%20Informations/EN/Pharma%20Solutions/03_030734e_Lutrol%20E%20-%20Liquid%20Grades.pdf; access date January 18, 2012.
42. C. F. Daher, G. M. Baroody and R. J. Howland, Effect of a surfactant, Tween 80, on the formation and secretion of chylomicrons in the rat, Food Chem. Toxicol. 41 (2003) 575-582; DOI: 10.1016/ S0278-6915(02)00299-5.10.1016/S0278-6915(02)00299-5
43. T. Tatsuishi, Y. Oyama, K. Iwase, J. Y. Yamaguchi, M. Kobayashi, Y. Nishimura, A. Kanada and S. Hirama, Polysorbate 80 increases the susceptibility to oxidative stress in rat thymocytes, Toxicology 207 (2005) 7-14; DOI: 10.1016/j.tox.2004.07.020.10.1016/j.tox.2004.07.02015590117
45. S. A. Tayel, I. I. Soliman and D. Louis, Improvement of dissolution properties of carbamazepine through application of the liquisolid tablet technique, Eur. J. Pharm. Biopharm. 69 (2008) 342-347; DOI: 10.1016/j.ejpb.2007.09.003.10.1016/j.ejpb.2007.09.00317949959
46. M. Saeedi, J. Akbari, K. Morteza-Semnani, R. Enayati-Fard, S.Sar-Reshteh-dar and A. Soleymani, Enhancement of dissolution rate of indomethacin using liquisolid compacts, Iran J. Pharm.Res. 10 (2011) 25-34.
47. V. B. Yadav and A. V. Yadav, Improvement of solubility and dissolution of indomethacin by liquisolid and compaction granulation technique, J. Pharm. Sci. Res. 1 (2009) 44-51.
48. Y. Javadzadeh, M. R. Siahi-Shadbad, M. Barzegar-Jalali and A. Nokhodchi, Enhancement of dissolution rate of piroxicam using liquisolid compacts, Il Farmaco 60 (2005) 361-365; DOI: 10. 1016/j.farmac.2004.09.005.10.1016/j.farmac.2004.09.00515848213
49. A. A. Elkordy, U. Bhangale, N. Murle and M. F. Zarara, Combination of lactose (as a carrier) with Cremophor® EL (as a liquid vehicle) to enhance dissolution of griseofulvin, Powder Technol. 246 (2013) 182-186; DOI: 10.1016/j.powtec.2013.05.024.10.1016/j.powtec.2013.05.024
50. B. Akinlade, A. A. Elkordy, E. A. Essa and S. Elhagar, Liquisolid systems to improve the dissolution of furosemide, Sci. Pharm. 78 (2010) 325-344; DOI: 10.3797/scipharm.0912-23.10.3797/scipharm.0912-23
51. C. C. Liao and C. I. Jarowski, Dissolution rates of corticoid solutions dispersed on silicas, J. Pharm.Sci. 73 (1984) 401-403; DOI: 10.1002/jps.2600730330.10.1002/jps.2600730330
52. A. A. Elkordy, X. N. Tan and E. A. Essa, Spironolactone release from liquisolid formulations prepared with CapryolTM 90, Solutol® HS-15 and Kollicoat® SR 30 D as non-volatile liquid vehicles, Eur. J. Pharm. Biopharm. 83 (2013) 203-223; DOI: 10.1016/j.ejpb.2012.08.004.10.1016/j.ejpb.2012.08.004
53. A. A. Elkordy, E. A. Essa, S. Dhuppad and P. Jammiqumpula, Liquisolid technique to enhance and to sustain griseofulvin dissolution: effect of choice of non-volatile liquid vehicles, Int. J. Pharm. 434 (2012) 122-132; DOI: 10.1016/j.ijpharm.2012.05.072.10.1016/j.ijpharm.2012.05.072
54. V. Agarwal, A. Siddiqui, H. Ali and S. Nazzal, Dissolution and power flow characterization of solid self-emulsified drug delivery system (SEDDS), Int. J. Pharm. 366 (2009) 44-52; DOI: 10. 1016/j.ijpharm.2008.08.046.10.1016/j.ijpharm.2008.08.046
55. G. Kahr and F. T. Madsen, Determination of the cation exchange capacity and the surface area of bentonite, illite and kaolinite by methylene blue absorption, Appl. Clay Sci. 9 (1995) 327-336; DOI: 10.1016/0169-1317(94)00028-O.10.1016/0169-1317(94)00028-O
56. M. Van Speybroeck, R. Mellaerts, R. Mols, T. D. Thi, J. A. Martens, J. Van Humbeeck, P. Annaert, G. Van den Mooter and P. Augistijns, Enhanced absorption of the poorly soluble drug fenofibrate by tuning its release rate from ordered mesoporous silica, Eur. J. Pharm. Sci. 41 (2010) 623-630; DOI: 10.1016/j.ejps.2010.09.002.10.1016/j.ejps.2010.09.00220850527
57. V. B. Yadav, A. B. Nighute, A. V. Yadav and S. B. Bhise, Aceclofenac size enlargement by non- -aqueous granulation with improved solubility and dissolution, Arch. Pharm. Sci. Res. 1 (2009) 115-122.
58. P. G. Manogar, B. N. V. Hari and D. R. Devi, Emerging liquisolid compact technology for solubility enhancement of BCS Class-II drug, J. Pharm. Sci. Res. 3 (2011) 1604-1611.
59. Fuji Chemical Industry Co., Ltd., Neusilin - Generel Properties, 2010; http://www.neusilin.com/product/general_properties.php; access date October 18, 2012.
60. C. M. Hentzschel, M. Alnaief, I. Smirnova, A. Sakmann and C. S. Leopold, Tableting properties of silica aerogels and other silicates, Drug Dev. Ind. Pharm. 38 (2012) 462-467; DOI: 10.3109/03639045.2011.611806.10.3109/03639045.2011.61180621961994
61. Fuji Chemical Industry Co., Ltd., Neusilin, 2011; http://www.fujichemical.co.jp/english/medical/ medicine/neusilin/index.html; access date October 18, 2012.
62. Fuji Chemical Industry Co., Ltd., The Specialty Excipient Neusilin®, 2009; http://www.harke. com/fileadmin/images/pharma/Broschueren/Fuji_Neusilin.pdf; access date January 18, 2012.
63. X. Zhao, Y. Q. Zhou, S. Potharaju, H. Lou, H. M. Sun, E. Brunson, H. Almoazen and J. Johnson, Development of a self micro-emulsifying tablet of cyclosporine-A by the liquisolid compact technique, Int. J. Pharm. Sci. Res. 2 (2011) 2299-2308.
64. B. Van Eerdenbrugh, L. Froyen, J. Van Humbeeck, J. A. Martens, P. Augustijns and G. Van Den Mooter, Alternative matrix formers for nanosupension solidification: Dissolution performance and X-ray microanalysis as an evaluation tool for powder dispersion, Eur. J. Pharm. Sci. 35 (2008) 344-353; DOI: 10.1016/j.ejps.2008.08.003.10.1016/j.ejps.2008.08.00318765282
65. M. J. Kang, S. Y. Jung, W. H. Song, J. S. Park, S. U. Choi, K. T. Oh, H. K. Choi, Y. W. Choi, J. Lee, B. J. Lee and S. C. Chi, Immediate release of ibuprofen from Fujicalin®-based fast-dissolving self-emulsifying tablets, Drug Dev. Ind. Pharm. 37 (2011) 1298-1305; DOI:10.3109/03639045.2011.571695.10.3109/03639045.2011.57169521476949
66. H. Schlack, A. Bauer-Brandl, R. Schubert and D. Becker, Properties of Fujicalin®, A new modified anhydrous dibasic calcium phosphate for direct compression: Comparison with dicalcium phosphate dihydrate, Drug Dev. Ind. Pharm. 27 (2001) 789-801.10.1081/DDC-100107242
67. Z. Wu, Y. Jiang, T. Kim and K. Lee, Effect of surface coating on the controlled release of vitamin B1 from mesoporous silica tablets, J. Control. Release 119 (2007) 215-221; DOI: 10.1016/j.jconrel. 2007.03.001.
68. T. Ukmar and O. Planin{ek, Ordered mesoporous silicates as matrices for controlled release of drugs, Acta Pharm. 60 (2010) 373-385; DOI: 10.2478/v1007-010-0037-4.10.2478/v1007-010-0037-421169131
69. M. Vallet-Regi, A. Ramila, R. P. del Rea and J. Pérez-Pariente, A new property of MCM-41: drug delivery system, Chem. Mater. 13 (2001) 308-311; DOI: 10.1021/cm0011559.70. R. Mellaerts, R. Mois, J. A. G. Jammaer, C. A. Aerts, P. Annaert, J. Van Humbeeck, G. Van den Mooter, P. Augustijns and J. A. Martens, Increasing the oral bioavailability of the poorly water soluble drug itraconazole with ordered mesoporous silica, Eur. J. Pharm. Biopharm. 69 (2008) 223-230; DOI: 10.1016/j.ejpb.2007.11.006.10.1016/j.ejpb.2007.11.00618164930
71. M. Vialpando, F. Backhuijs, J. A. Martens and G. Van den Mooter, Risk assessment of premature drug release during wet granulation of ordered mesoporous silica loaded with poorly soluble compounds intraconazole, fenofibrate, naproxen, and ibuprofen, Eur. J. Pharm. Biopharm. 81 (2012) 190-198; DOI: 10.1016/j.ejpb.2012.01.012.10.1016/j.ejpb.2012.01.01222306694
72. T. Heikkilä, J. Salonen, J. Tuura, N. Kumar, T. Salmi, D. Y. Murzin, M. S. Hamdy, G. Mul, L. Laitinen, A. M. Kaukonen, J. Hirvonen and V. P. Lehto, Evaluation of mesoporous TCPSi, MCM-41, SBA-15 and TUD-1 materials as API carriers for oral drug delivery, Drug Deliv. 14 (2007) 337-347; DOI: 10.1080/10717540601098823.10.1080/1071754060109882317701523
73. M. Van Speybroeck, V. Barillaro, T. D. Thi, R. Mellaerts, J. Martens, J. Van Humbeeck, J. Vermant, P. Annaert, G. Van den Mooter and P. Augustijns, Ordered mesoporous silica material SBA-15: a broad-spectrum formulation platform for poorly soluble drugs, J. Pharm. Sci. 98 (2009) 2648-2658; DOI: 10.1002/jps.21638.10.1002/jps.2163819072861
74. B. Chen, G. Quan, Z. Wang, J. Chen, L. Wu, Y. Xu, G. Li and C. Wu, Hollow mesoporoussilicas as a drug solution delivery system for insoluble drugs, Powder Technol. 240 (2013) 48-53; DOI: 10.1016/j.powtec.2012.07.008.10.1016/j.powtec.2012.07.008
76. K. M. El-Say, A. M. Samy and M. I. Fetouh, Formulation and evaluation of rofecoxib liquisolid tablets, Int. J. Pharm. Sci. Rev. Res. 3 (2010) 135-142.
78. A. Sheth and C. I. Jarowski, Use of powdered solutions to improve the dissolution rate of polythiazide tablets, Drug Dev. Ind. Pharm. 16 (1990) 769-777; DOI: 10.3109/03639049009114908.10.3109/03639049009114908
79. E. B. Basalious, W. El-Sebaie and O. El-Gazayerly, Rapidly absorbed orodispersible tablet containing molecularly dispersed felodipine for management of hypertensive crisis: Development, optimization and in vitro/in vivo studies, Pharm. Dev. Technol. 18 (2013) 407-416; DOI: 10.3109/
80. S. S. Spireas, C. I. Jarowski and B. D. Rohera, Powdered solution technology: Principles and mechanism, Pharm. Res. 9 (1992) 1351-1358; DOI: 10.1023/A:1015877905988.10.1023/A:1015877905988
81. M. Khanfar, S. M. Sheikh and R. Hawari, Formulation factors affecting the release of ezetimibe from different liquisolid compacts, Pharm. Dev. Technol. 18 (2013) 417-427; DOI: 10.3109/10837450.2012.680594.10.3109/10837450.2012.680594
84. K. Rajesh, R. Rajalakshmi, J. Umamaheswari and C. K. A. Kumar, Liquisolid technique: a novel approach to enhance solubility and bioavailability, Int. J. Biopharm. 2 (2011) 8-13.
85. R.Grover, S. Spireas and C. Lau-Cam, Development of a simple spectrophotometric method for propylene glycol detection in tablets, J. Pharm. Biomed. Anal. 16 (1998) 931-938; DOI: 10.1016/ S0731-7085(97)00098-8.10.1016/S0731-7085(97)00098-8
86. R. Boghra, A. Patel, H. Desai and A. Jadhav, Formulation and evaluation of irbesartan liquisolid tablets, Int. J. Pharm. Sci. Rev. Res. 9 (2011) 32-37.
87. S. V. Kasture, S. B. Gondkar, A. B. Darekar, D. Priyobrata and K. V. Bhambar, Enhancement of dissolution rate of lansoprazole using liquisolid tablet technique, Int. J. Pharm. Res. 3 (2011) 27-31.
88. M. A. Hassan and H. M. El-Saghir, Enhancement of dissolution and the anti-inflammatory effect of nimesulide, using liquisolid compact for oral appliccation, Bull. Pharm. Sci. 34 (2011) 1-8. 10.1248/bpb.34.1
89. The European Directorate for the Quality of Medicines & Health Care, European Pharmacopoeia 7.2, 2011; http://online6.edqm.eu/ep702/; access date February 18, 2012.
90. D. C. Bibby, N. M. Davies and I. G. Tucker, Mechanisms by which cyclodextrins modify drug release from polymeric drug delivery systems, Int. J. Pharm. 197 (2000) 1-11; DOI: 10.1016/S0378-5173(00)00335-5.10.1016/S0378-5173(00)00335-5
92. A. Nokhodchi, C. M. Hentzschel and C. S. Leopold, Drug release from liquisolid systems: speed it up, slow it down, Expert Opin. Drug Deliv. 8 (2011) 191-205; DOI: 10.1517/17425247.2011.548801.10.1517/17425247.2011.54880121222556
93. A. Panda and D. M. Biyani, Studies on liquisolid system as a technique to modify the dissolution rate of nefedipine, Am. J. Pharmtech. Res. 3 (2013) 686-698.
94. N. Chella, N. Shastri and R. R. Tadikonda, Use of the liquisolid compact technique for improvement of the dissolution rate of valsartan, Acta Pharm. Sin B. 2 (2012) 502-508; DOI: 10.1016/j. apsb.2012.07.005..
95. N. Thakur, S. L. Khokra, D. Sharma, N. S. Thakur, R. Purohit and V. Arya, A review on pharmaceutical application of liquisolid technique, Am. J. Pharmtech. Res. 1 (2011) 1-18.