Kale A A, Torchilin V P
Department of Pharmaceutical Sciences and Center for Pharmaceutical Biotechnology and Nanomedicine, Northeastern University, Boston, MA 02115, USA.
Polym Sci Ser A Chem Phys. 2009 Jun;51(6):730-737. doi: 10.1134/S0965545X09060182.
Polyethylene glycol derivatives, such as block copolymers of polyethylene glycol and diacyllipids (for example, phosphatidylethanolamine) are widely used for surface modification of various pharmaceutical carriers in order to impart them longevity in the body. To make polyethylene glycol detachable from the surface of pharmaceutical carrier and facilitate the interaction of the carrier with target cells when in pathological zone, we have prepared a set of polyethylene glycol-phosphatidylethanolamine block copolymers with the pH sensitive hydrazone bond between polyethylene glycol and phosphatidylethanolamine, which destabilizes at lowered pH values typical for tumors and inflammation zones. We have demonstrated that the stability of the hydrazone bond at normal physiological pH (7.4) as well as the rate of its hydrolysis at pH 6 and below strongly depend on the type of substitutions at this bond. Using aliphatic and aromatic aldehydes and ketones, polyethylene glycol-phosphatidylethanolamine block copolymers were prepared with different stabilities and degradation rates, which can be useful in constructing stimuli-sensitive pharmaceutical carriers.
聚乙二醇衍生物,如聚乙二醇与二酰基脂质(例如磷脂酰乙醇胺)的嵌段共聚物,被广泛用于各种药物载体的表面修饰,以便赋予它们在体内的长效性。为了使聚乙二醇能够从药物载体表面脱离,并在处于病理区域时促进载体与靶细胞的相互作用,我们制备了一组聚乙二醇 - 磷脂酰乙醇胺嵌段共聚物,其在聚乙二醇和磷脂酰乙醇胺之间具有pH敏感的腙键,该键在肿瘤和炎症区域典型的较低pH值下会不稳定。我们已经证明,腙键在正常生理pH(7.4)下的稳定性以及在pH 6及以下时的水解速率强烈依赖于该键处的取代类型。使用脂肪族和芳香族醛和酮,制备了具有不同稳定性和降解速率的聚乙二醇 - 磷脂酰乙醇胺嵌段共聚物,这对于构建刺激敏感型药物载体可能是有用的。