[1]
Yagi, N.; Terashima, Y.; Kenmotsu, H.; Sekikawa, H.; Takada, M. Dissolution behavior of probucol from solid dispersion systems of probucol polyvinylpyrrolidone. Chem. Pharm. Bull. (Tokyo), 1996, 44, 241-244.
[2]
Heel, R.C.; Brogden, R.N.; Speight, T.M.; Avery, G.S. Probucol: A review of its pharmacological properties and therapeutic use in patients with hypercholesterolemia. Drugs, 1978, 15, 409-428.
[3]
Li, G.; Yin, L.; Liu, T.; Zheng, X.; Xu, G.; Xu, Y.; Yuan, R.; Che, J.; Liu, H.; Zhou, L.; Chen, X.; He, M.; Li, Y.; Wu, L.; Liu, E. Role of probucol in preventing contrast-induced acute kidney injury after coronary interventional procedure. Am. J. Cardiol., 2009, 103, 512-514.
[4]
Liu, G.X.; Ou, D.M.; Li, L.X.; Chen, L.X.; Huang, H.L.; Liao, D.F.; Tang, C.S. Probucol inhibits oxidized-low density lipoprotein-induced adhesion of monocytes to endothelial cells in vitro. Acta Pharmacol. Sin., 2002, 23, 516-522.
[5]
Yamashita, S.; Matsuzawa, Y. Where are we with probucol: A new life for an old drug? Atherosclerosis, 2009, 207, 16-23.
[6]
Champagne, D.; Pearson, D.; Dea, D.; Rochford, J.; Poirier, J. The cholesterol-lowering drug probucol increases apolipoprotein E production in the hippocampus of aged rats: Implications for Alzheimer’s disease. Neuroscience, 2003, 121, 99-110.
[7]
Poirier, J. Apolipoprotein E and cholesterol metabolism in the pathogenesis and treatment of Alzheimer’s disease. Trends Mol. Med., 2003, 9, 94-101.
[8]
Endo, K.; Miyashita, Y.; Sasaki, H.; Ohira, M.; Saiki, A.; Koide, N.; Otsuka, M.; Oyama, T.; Takeyoshi, M.; Ito, Y.; Shirai, K. Probucol delays progression of diabetic nephropathy. Diabetes Res. Clin. Pract., 2006, 71, 156-163.
[9]
Zhou, G.; Wang, Y.; He, P.; Li, D. Probucol inhibited Nox2 expression and attenuated podocyte injury in type 2 diabetic nephropathy of db/db mice. Biol. Pharm. Bull., 2013, 36, 1883-1890.
[10]
Bagdade, J.D.; Lane, J.T.; Subbaiah, P.V. Probucol normalizes cholesteryl ester transfer in type 2 diabetes. Diabetes Res. Clin. Pract., 2016, 116, 29-35.
[11]
Gorogawa, S.; Kajimoto, Y.; Umayahara, Y.; Kaneto, H.; Watada, H.; Kuroda, A.; Kawamori, D.; Yasuda, T.; Matsuhisa, M.; Yamasaki, Y.; Hori, M. Probucol preserves pancreatic beta-cell function through reduction of oxidative stress in type 2 diabetes. Diabetes Res. Clin. Pract., 2002, 7, 1-10.
[12]
Liu, J.H.; Liu, D.F.; Wang, N.N.; Lin, H.L.; Mei, X. Possible role for the thioredoxin system in the protective effects of probucol in the pancreatic islets of diabetic rats. Clin. Exp. Pharmacol. Physiol., 2011, 38(8), 528-533.
[13]
Iqbal, M.; Okazaki, Y.; Okada, S. Probucol modulates iron nitrilotriacetate (Fe-NTA)-dependent renal carcinogenesis and hyperproliferative response: Diminution of oxidative stress. Mol. Cell. Biochem., 2007, 304, 61-69.
[14]
Jiang, Y.S.; Lei, J.A.; Feng, F.; Liang, Q.M.; Wang, F.R. Probucol suppresses human glioma cell proliferation in vitro via ROS production and LKB1-AMPK activation. Acta Pharmacologica Sinica, 2014, 35, 1556-1565.
[15]
Shudo, J.; Pongpeerapat, A.; Wanawongthai, C.; Moribe, K.; Yamamoto, K. In vivo assessment of oral administration of probucol nanoparticles in rats. Biol. Pharm. Bull., 2008, 31, 321-325.
[16]
Taha, E.; Ghorab, D.; Zaghloul, A. Bioavailability assessment of vitamin A self-nano emulsified drug delivery systems in rats: A comparative study. Med. Princ. Pract., 2007, 16, 355-359.
[17]
Nielsen, F.S.; Petersen, K.B.; Mullertz, A. Bioavailability of probucol from lipid and surfactant based formulations in minipigs: Influence of droplet size and dietary state. Eur. J. Pharm. Biopharm., 2008, 69, 553-562.
[18]
Zaghloul, A.; Abd-Allah, F.; Abu Seada, H.; Nada, A. Stability and human bioavailability of optimized self-emulsified drug delivery system of ibuprofen. Am. J. Pharm. Tech. Res, 2013, 3, 721-733.
[19]
Han, L.; Yang, Q.; Shen, T.; Qing, J.; Wang, J. Lymphatic transport of orally administered probucol-loaded mPEG-DSPE micelles. Drug Deliv., 2016, 23, 1955-1961.
[20]
Zaghloul, A.; Khattab, I.; Nada, A.; Al-Saidan, S. Preparation, characterization and optimization of probucol self-emulsified drug delivery system to enhance solubility and dissolution. Pharmazie, 2008, 63, 654-660.
[21]
Danafar, H.; Hamidi, M. Simple and sensitive high-performance liquid chromatography (HPLC) method with UV detection for mycophenolic acid assay in human plasma. Application to a bioequivalence study. Adv. Pharm. Bull., 2015, 5(4), 563-568.
[22]
Danafar, H.; Hamidi, M. Pharmacokinetics and bioequivalence study of amlodipine and atorvastatin in healthy male volunteers by LC-MS. Pharm. Sci., 2015, 21(Suppl. 1), 167-174C.
[23]
Ueyama, E.; Tamura, K.; Mizukawa, K.; Kano, K. Realistic prediction of solid pharmaceutical oxidation products by using a novel forced oxidation system. J. Pharm. Sci., 2014, 103, 1184-1193.
[24]
Komoda, M.; Onuki, N.; Harada, I. Studies on cause of color reversion of edible soybean oil and its prevention Part II. Tocored as a precursor of color reversion of soybean oil. Agric. Biol. Chem., 1967, 31(4), 461-469.
[25]
Kubo, Y.; Yagi, N.; Sekikawa, H. Stability of probucol-polyvinylpyrrolidone solid dispersion systems. Yakugaku Zasshi – J. Pharm. Soc. Japan, 2011, 131, 629-634.
[26]
Palin, K.J.; Wilson, C.G. The effect of different oils on the absorption of probucol in the rat. J. Pharm. Pharmacol., 1984, 36, 641-643.
[27]
Bardelmeijer, H.A.; Ouwehand, M.; Malingre, M.M.; Schellens, J.H.; Beijnen, J.H. van, O.T. Entrapment by Cremophor EL decreases the absorption of paclitaxel from the gut. Cancer Chemother. Pharmacol., 2002, 49, 119-125.
[28]
Malingre, M.M.; Schellens, J.H.; Tellingen, O.; van Ouwehand, M.; Bardelmeijer, H.A.; Rosing, H.; Koopman, F.J.; Schot, M.E. Ten, Bokkel, Huinink, W.W.; Beijnen, J.H. The co-solvent Cremophor EL limits absorption of orally administered paclitaxel in cancer patients. Br. J. Cancer, 2001, 85, 1472-1477.
[29]
Porter, C.J.; Kaukonen, A.M.; Boyd, B.J.; Edwards, G.A.; Charman, W.N. Susceptibility to lipase-mediated digestion reduces the oral bioavailability of danazol after administration as a medium-chain lipid-based microemulsion formulation. Pharm. Res., 2004, 2, 1405-1412.
[30]
Holm, R.; Porter, C.J.; Edwards, G.A.; Mullertz, A.; Kristensen, H.G.; Charman, W.N. Examination of oral absorption and lymphatic transport of halofantrine in a triple-cannulated canine model after administration in self-microemulsifying drug delivery systems (SMEDDS) containing structured triglycerides. Eur. J. Pharm. Sci., 2003, 20, 91-97.
[31]
Yamamoto, K.; Fukuda, N.; Shiroi, S.; Shiotsuki, Y.; Nagata, Y.; Tani, T.; Sakai, T. Effects of dietary fat levels on the absorption and tissue accumulation of probucol in the rat. Arzneimittelforschung, 1994, 44, 1059-1062.