Amino Acids in the Development of Prodrugs

被引:63
作者
Vale, Nuno [1 ,2 ,3 ,4 ]
Ferreira, Abigail [1 ,5 ]
Matos, Joana [6 ]
Fresco, Paula [1 ]
Gouveia, Maria Joao [3 ,4 ]
机构
[1] Univ Porto, Pharmacol Lab, Dept Drug Sci, Fac Pharm, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[2] Univ Porto IPATIMUP, Inst Mol Pathol & Immunol, Rua Julio Amaral de Carvalho 45, P-4200135 Porto, Portugal
[3] Univ Porto, Inst Invest & Inovacao Saude i3S, Rua Alfredo Allen 208, P-4200135 Porto, Portugal
[4] Univ Porto, Inst Biomed Sci Abel Salazar ICBAS, Dept Mol Pathol & Immunol, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[5] Univ Porto, Fac Pharm, Dept Chem Sci, LAQV&REQUIMTE,Lab Appl Chem, Rua Jorge Viterbo Ferreira 228, P-4050313 Porto, Portugal
[6] SpiroChem AG, Rosental Area, WRO 1074-3,Mattenstr 24, CH-4058 Basel, Switzerland
来源
MOLECULES | 2018年 / 23卷 / 09期
关键词
amino acid transport; drug delivery; prodrug design; stability studies; in vitro and in vivo assays; NEUTRON-CAPTURE THERAPY; PLASMA-PROTEIN-BINDING; WATER-SOLUBLE PRODRUG; IN-VIVO EVALUATION; ESTER PRODRUGS; DRUG-DELIVERY; DIPEPTIDE PRODRUGS; LISDEXAMFETAMINE DIMESYLATE; PHYSICOCHEMICAL PROPERTIES; INTRATHECAL STRYCHNINE;
D O I
10.3390/molecules23092318
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although drugs currently used for the various types of diseases (e.g., antiparasitic, antiviral, antibacterial, etc.) are effective, they present several undesirable pharmacological and pharmaceutical properties. Most of the drugs have low bioavailability, lack of sensitivity, and do not target only the damaged cells, thus also affecting normal cells. Moreover, there is the risk of developing resistance against drugs upon chronic treatment. Consequently, their potential clinical applications might be limited and therefore, it is mandatory to find strategies that improve those properties of therapeutic agents. The development of prodrugs using amino acids as moieties has resulted in improvements in several properties, namely increased bioavailability, decreased toxicity of the parent drug, accurate delivery to target tissues or organs, and prevention of fast metabolism. Herein, we provide an overview of models currently in use of prodrug design with amino acids. Furthermore, we review the challenges related to the permeability of poorly absorbed drugs and transport and deliver on target organs.
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页数:61
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