References
- Lipinski, C. A. L. F. Poor Aqueous Solubility-an Industry-Wide Problem in Drug Discovery. Am. Pharm. Rev. 2002, 5, 82–85.
- Gurram, A. K.; Deshpande, P. B.; Kar, S. S.; Nayak, U. Y.; Udupa, N.; Reddy, M. S. Role of Components in the Formation of Self-microemulsifying Drug Delivery Systems. Indian J. Pharm. Sci. 2015, 77, 249–257.
- Dahan, A.; Miller, J. M.; Amidon, G. L. Prediction of Solubility and Permeability Class Membership: Provisional BCS Classification of the World’s Top Oral Drugs. AAPS J. 2009, 11, 740–746. DOI: https://doi.org/10.1208/s12248-009-9144-x.
- Papdiwal, A.; Pande, V.; Sagar, K. Design and Characterization of Zaltoprofen Nanosuspension by Precipitation Method. Der. Pharm. Chem. 2014, 6, 161.
- Kumar, A.; Sahoo, S. K.; Padhee, K.; Kochar, P. S.; Sathapathy, A.; Pathak, N. Review of Solubility Enhancement Techniques for Hydrophobic Drugs. Pharm. Globale. 2011, 3, 001–007.
- Tao, C.; Huo, T.; Zhang, M.; Chen, Z.; Zhang, X.; Song, H. Evaluation of the Stability and Absorption of Tacrolimus Self-Microemulsifying Drug Delivery System. J. Drug Deliv. Sci. Technol. 2020, 57, 101640. DOI: https://doi.org/10.1016/j.jddst.2020.101640.
- Man, N.; Wang, Q.; Li, H.; Adu-Frimpong, M.; Sun, C.; Zhang, K.; Yang, Q.; Wei, Q.; Ji, H.; Toreniyazov, E.; et al. Improved Oral Bioavailability of Myricitrin by Liquid Self-Microemulsifying Drug Delivery Systems. J. Drug Deliv. Sci. Technol. 2019, 52, 597–606. DOI: https://doi.org/10.1016/j.jddst.2019.05.003.
- Tang, H. B.; Inoue, A.; Oshita, K.; Hirate, K.; Nakata, Y. Zaltoprofen Inhibits Bradykinin-Induced Responses by Blocking the Activation of Second Messenger Signaling Cascades in Rat Dorsal Root Ganglion Cells. Neuropharmacology 2005, 48, 1035–1042. DOI: https://doi.org/10.1016/j.neuropharm.2005.01.011.
- Krishna, E. H.; Gupta, V. R. M.; Jyothi, S. Spherical Crystallization of Zaltoprofen for Enhancement of Micrometric Properties and Dissolution Rate. Int. J. Pharm. Sci. Res. 2012, 3, 2024.
- Panzade, P.; Shendarkar, G. Superior Solubility and Dissolution of Zaltoprofen via Pharmaceutical Cocrystals. Turk. J. Pharm. Sci. 2019, 16, 310–316. DOI: https://doi.org/10.4274/tjps.galenos.2018.15013.
- Chatap, V. K.; Marathe, G. M.; Maurya, A. R.; Patil, N. D. Formulation and Evaluation of Zaltoprofen Fast Disintegrating Tablet. J. PharmaSciTech. 2013, 3, 20.
- Hazzaa, S. A.; Abd-Alhameed, S. N. Formulation and Evaluation of Optimized Zaltoprofen Lyophilized Tablets by Zydis Technique. Iraqi J. Pharm. Sci. 2017, 26, 40–49.
- Mishra, R.; Prabhavalkar, K. S.; Bhatt, L. K. Preparation, Optimization, and Evaluation of Zaltoprofen-loaded Microemulsion and Microemulsion-based Gel for Transdermal Delivery. J. Liposome Res. 2016, 26, 297–306. DOI: https://doi.org/10.3109/08982104.2015.1120746.
- Kalamkar, R.; Wadher, S. Formulation and Pharmacokinetic Evaluation of Phosal Based Zaltoprofen Solid Self-Nanoemulsifying Drug Delivery System. Pharm. Nanotechnol. 2019, 7, 328–338. DOI: https://doi.org/10.2174/2211738507666190802141754.
- Aggarwal, G.; Harikumar, S.; Jaiswal, P.; Singh, K. Development of Self-Micro Emulsifying Drug Delivery System, and Solid-Self-Micro Emulsifying Drug Delivery System of Telmisartan. Int. J. Pharma. Investig. 2014, 4, 195–206. DOI: https://doi.org/10.4103/2230-973X.143123.
- Jangipuria, F.; Londhe, V. Solubility Enhancement of Lurasidone Hydrochloride by Preparing SMEDDS. Int. J. Pharm. Pharm. Sci. 2015, 7, 283–288.
- Amdekar, S.; Roy, P.; Singh, V.; Kumar, A.; Singh, R.; Sharma, P. Anti-Inflammatory Activity of Lactobacillus on Carrageenan-Induced Paw Edema in Male Wistar Rats. Int. J. Inflamm. 2012, 2012, 1–6. DOI: https://doi.org/10.1155/2012/752015.
- Baek, M. K.; Lee, J. H.; Cho, Y. H.; Kim, H. H.; Lee, G. W. Self-microemulsifying Drug-delivery System for Improved Oral Bioavailability of Pranlukast Hemihydrate: Preparation and Evaluation. Int. J. Nanomedicine. 2013, 8, 167–176.
- Prajapati, S.; Joshi, H.; Patel, C. Preparation and Characterization of Self-Microemulsifying Drug Delivery System of Olmesartan Medoxomil for Bioavailability Improvement. J. Pharm. 2013, 2013, 728425.