Hirabayashi Hideki, Fujisaki Jiro
Biopharmaceutical and Pharmacokinetic Research Laboratories, Fujisawa Pharmaceutical Company, Osaka, Japan.
Clin Pharmacokinet. 2003;42(15):1319-30. doi: 10.2165/00003088-200342150-00002.
Despite several decades of progress, bone-specific delivery is still limited by the unique anatomical features of bone, which mainly consists of inorganic hydroxyapatite. A practical approach to this problem is to produce targeted drugs that have a high affinity for hydroxyapatite. Bisphosphonates are a class of synthetic compounds structurally related to pyrophosphate. Bisphosphonates rapidly localise on the bone surface after being administered either intravenously or orally, since the P-C-P portion of the bisphosphonate structure has high affinity for hydroxyapatite. Therefore, bisphosphonate modification might be a promising method for targeting drugs selectively to the bone. Bisphosphonate-conjugated drugs are hydrophilic and highly water-soluble due to the acidic nature of the bisphosphonate moiety at physiological pH, and therefore they hardly permeate through the biological membrane of soft tissues. These physicochemical changes also reduce the intrinsic susceptibility of the drug to metabolism, promoting urinary or biliary excretion as unchanged drug. All these physicochemical and pharmacokinetic alterations contribute to the exceptional skeletal disposition of bisphosphonate-conjugated drugs. Bisphosphonate conjugation is based on chemical modification of the targeting molecule, and therapeutically optimised bisphosphonate derivatives have to be custom-developed on a case-by-case basis. The bisphosphonate moiety is usually coupled with the targeting drug through a specific linkage. The high affinity of bisphosphonate conjugates for the bone is not simply dependent on the bisphosphonate moiety but on the resultant molecule as a whole, including the linker and the linked drug. Lipophilicity (represented as log P) appears to be an appropriate index for predicting the osteotropic properties of bisphosphonate derivatives. Several strategies using bisphosphonate-conjugated drugs have been investigated at a laboratory level with the aim of obtaining therapeutically optimised treatments for conditions such as osteoporosis, osteoarthritis and bone cancer. In each case, the intention is to achieve prolonged local exposure to high concentrations of the targeting drug, thereby improving therapeutic index by enhancing pharmacological efficacy and minimising systemic adverse effects. Although most examples of bone-specific drug delivery via bone-seeking agents still remain in preclinical studies, several phosphonate-coupled radiopharmaceuticals, such as samarium-153 complexed to tetraphosphonate, are expected to be an effective pain palliation therapies for metastatic bone cancer and are currently being developed in clinical trials. Furthermore, recent reports on bisphosphonate-modified proteins have illustrated the feasibility of bone-specific delivery of biologically active protein drugs, such as cytokines and growth factors.
尽管经过了几十年的发展,但骨特异性递送仍受到骨独特解剖结构的限制,骨主要由无机羟基磷灰石组成。解决这一问题的一个切实可行的方法是制备对羟基磷灰石具有高亲和力的靶向药物。双膦酸盐是一类结构上与焦磷酸盐相关的合成化合物。双膦酸盐经静脉或口服给药后会迅速在骨表面定位,因为双膦酸盐结构中的P-C-P部分对羟基磷灰石具有高亲和力。因此,双膦酸盐修饰可能是一种将药物选择性靶向至骨的有前景的方法。由于双膦酸盐部分在生理pH下呈酸性,双膦酸盐缀合药物具有亲水性且高度水溶性,因此它们很难透过软组织的生物膜。这些物理化学变化也降低了药物对代谢的内在敏感性,促进其以原形药物经尿液或胆汁排泄。所有这些物理化学和药代动力学改变都促成了双膦酸盐缀合药物独特的骨骼分布。双膦酸盐缀合是基于靶向分子的化学修饰,治疗上优化的双膦酸盐衍生物必须根据具体情况定制开发。双膦酸盐部分通常通过特定的连接键与靶向药物偶联。双膦酸盐缀合物对骨的高亲和力不仅简单地取决于双膦酸盐部分,还取决于整个所得分子,包括连接键和连接的药物。亲脂性(以log P表示)似乎是预测双膦酸盐衍生物骨趋向性性质的一个合适指标。在实验室层面已经研究了几种使用双膦酸盐缀合药物的策略,目的是为骨质疏松症、骨关节炎和骨癌等病症获得治疗上优化的治疗方法。在每种情况下,目的都是实现靶向药物在局部的长时间高浓度暴露,从而通过增强药理疗效和最小化全身不良反应来提高治疗指数。尽管通过趋骨性药物进行骨特异性药物递送的大多数实例仍处于临床前研究阶段,但几种膦酸盐偶联的放射性药物,如与四膦酸盐络合的钐-153,有望成为转移性骨癌的有效止痛疗法,目前正在进行临床试验开发。此外,最近关于双膦酸盐修饰蛋白质的报道说明了生物活性蛋白药物,如细胞因子和生长因子进行骨特异性递送的可行性。