Goldberg I, Kolker A E, Kass M A, Becker B
Aust J Ophthalmol. 1980 May;8(2):147-50. doi: 10.1111/j.1442-9071.1980.tb01673.x.
Pro-drugs are agents that require biotransformation prior to exhibiting pharmacologic activity. Dipivefrin (dipivalyl epinephrine or DPE) is an epinephrine pro-drug produced by the addition of two pivalic acid groups to the parent compound. This creates a more lipophilic molecule which penetrates the cornea more readily than epinephrine. Enzymes in ocular tissues convert dipivefrin into its active form, epinephrine. In concentrations approximately one-tenth that of epinephrine, topically applied dipivefrin therefore produces: (1) similar intra-ocular concentrations of epinephrine; (2) similar reductions in intra-ocular pressure (IOP); (3) similar degrees of mydriasis; and (4) fewer extraocular and systemic side effects. For reasons that are discussed, dipivefrin should probably not be used in conjunction with anticholinesterases. Dipivefrin offers the same risk of cystoid macular oedema as does epinephrine. Dipivefrin is a safe, effective, and well-tolerated alternative to epinephrine in the treatment of elevated IOP. It is particularly useful for patients who cannot tolerate epinephrine.
前体药物是在展现出药理活性之前需要进行生物转化的药物。地匹福林(双特戊酰肾上腺素或DPE)是一种通过在母体化合物上添加两个特戊酸基团而产生的肾上腺素前体药物。这产生了一个更具亲脂性的分子,它比肾上腺素更容易穿透角膜。眼组织中的酶将地匹福林转化为其活性形式肾上腺素。因此,以大约肾上腺素浓度十分之一的浓度局部应用地匹福林会产生:(1)相似的眼内肾上腺素浓度;(2)相似的眼内压(IOP)降低;(3)相似程度的瞳孔散大;以及(4)较少的眼外和全身副作用。出于已讨论的原因,地匹福林可能不应与抗胆碱酯酶药物联合使用。地匹福林与肾上腺素具有相同的黄斑囊样水肿风险。在治疗眼压升高方面,地匹福林是一种安全、有效且耐受性良好的肾上腺素替代药物。它对不能耐受肾上腺素的患者特别有用。