1,4-Dihydropyridine Antihypertensive Drugs: Recent Advances in Photostabilization Strategies

被引:66
作者
De Luca, Michele [1 ]
Ioele, Giuseppina [1 ]
Ragno, Gaetano [1 ]
机构
[1] Univ Calabria, Dept Pharm Hlth & Nutr Sci, I-87036 Arcavacata Di Rende, Italy
来源
PHARMACEUTICS | 2019年 / 11卷 / 02期
关键词
1,4-dihydropyridines; photostabilization; liposomes; cyclodextrins; light-absorbing excipients; opaque containers; nanosystems; CALCIUM-CHANNEL BLOCKERS; INCLUSION COMPLEXES; DERIVATIVE SPECTROPHOTOMETRY; PHOTODEGRADATION PRODUCT; BETA-CYCLODEXTRIN; STABILITY; FORMULATION; ISRADIPINE; NIFEDIPINE; NIMODIPINE;
D O I
10.3390/pharmaceutics11020085
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 1,4-dihydropyridine (DHP) drugs are nowadays the most used drugs in the treatment of hypertension. However, all the structures in this series present a significant sensitivity to light, leading to the complete loss of pharmacological activity. This degradation is particularly evident in aqueous solution, so much so that almost all DHP drugs on the market are formulated in solid preparations, especially tablets. The first and main process of photodegradation consists in the aromatization of the dihydropyridine ring, after which secondary processes can take place on the various substituents. A potential danger can result from the formation of single oxygen and superoxide species that can in turn trigger phototoxic reactions. Several strategies for the photostabilisation of DHP drugs have been proposed in recent years, in particular with the aim to formulate these drugs in liquid preparations, as well as to limit any toxicity problems related to light degradation. This review summarizes and describes the main aspects of the studies conducted in recent years to obtain photostable formulations of DHP drugs.
引用
收藏
页数:13
相关论文
共 61 条
[1]  
[Anonymous], 1998, DRUGS PHOTOCHEMISTRY
[2]   PHOTODEGRADATION OF NIMODIPINE AND FELODIPINE IN MICROHETEROGENEOUS SYSTEMS [J].
Brito, Julio ;
Pozo, Andres ;
Garcia, Cristobal ;
Nunez-Vergara, Luis J. ;
Morales, Javier ;
Guenther, German ;
Pizarro, Nancy .
JOURNAL OF THE CHILEAN CHEMICAL SOCIETY, 2012, 57 (03) :1313-1317
[3]  
Caritá AC, 2018, CURR MED CHEM, V25, P606, DOI 10.2174/0929867324666171009120154
[4]   1,4-Dihydropyridine Scaffold in Medicinal Chemistry, The Story So Far And Perspectives (Part 2): Action in Other Targets and Antitargets [J].
Carosati, E. ;
Ioan, P. ;
Micucci, M. ;
Broccatelli, F. ;
Cruciani, G. ;
Zhorov, B. S. ;
Chiarini, A. ;
Budriesi, R. .
CURRENT MEDICINAL CHEMISTRY, 2012, 19 (25) :4306-4323
[5]   Synthesis and Characterization of Impurities of Barnidipine Hydrochloride, an Antihypertensive Drug Substance [J].
Cheng, Zhi-Gang ;
Dai, Xu-Yong ;
Li, Li-Wei ;
Wan, Qiong ;
Ma, Xiang ;
Xiang, Guang-Ya .
MOLECULES, 2014, 19 (01) :1344-1352
[6]  
Coca A, 2013, EXPERT REV CARDIOVAS, V11, P91, DOI [10.1586/ERC.12.155, 10.1586/erc.12.155]
[7]  
Commission E.P., 2018, EUR PHARM 9 5
[8]   Cyclodextrins as excipients in tablet formulations [J].
Conceicao, Jaime ;
Adeoye, Oluwatomide ;
Cabral-Marques, Helena Maria ;
Sousa Lobo, Jose Manuel .
DRUG DISCOVERY TODAY, 2018, 23 (06) :1274-1284
[9]   Cyclodextrins, from molecules to applications [J].
Crini, Gregorio ;
Fourmentin, Sophie ;
Fenyvesi, Eva ;
Torri, Giangiacomo ;
Fourmentin, Marc ;
Morin-Crini, Nadia .
ENVIRONMENTAL CHEMISTRY LETTERS, 2018, 16 (04) :1361-1375
[10]   Potential of Liposomes for Enhancement of Oral Drug Absorption [J].
Daeihamed, Marjan ;
Dadashzadeh, Simin ;
Haeri, Azadeh ;
Akhlaghi, Masoud Faghih .
CURRENT DRUG DELIVERY, 2017, 14 (02) :289-303