Nguyen Trung Dinh, Nguyen The Ngoc, Nguyen Trang Thuy Thi, Ivanov Igor A, Nguyen Khoa Cuu, Tran Quyen Ngoc, Hoang Anh Ngoc, Utkin Yuri N
Institute of Research and Development, Duy Tan University, Da Nang City 550000, Vietnam.
Institute of Applied Materials Science, Vietnam Academy of Science and Technology, Ho Chi Minh City 700000, Vietnam.
Nanomaterials (Basel). 2019 Aug 23;9(9):1191. doi: 10.3390/nano9091191.
It is well-known that drugs administered into an organism intravenously or through the gastrointestinal tract are degraded by enzymes of the body, reducing their therapeutic effect. One of the ways to decrease this undesirable process is through the inclusion of drugs in nanomaterials. Earlier strong anticoagulant activity was demonstrated for dipeptide IleTrp (IW) and adenosine (Ado). In this work, the effect of inclusion in nanomaterials on the biological activity of IW and Ado was studied. For this purpose, Ado and IW were incorporated into thermosensitive nanogel composed of pluronic P123-grafted heparin. The prepared nanocarrier was characterized by transmission electron microscopy, dynamic light scattering, and ζ-potential. Biological activity was determined by measuring the bleeding time from mouse tail in vivo and the time of clot formation in vitro. It was found that encapsulation of Ado and IW into nanomaterial significantly increased their effects, resulting in an increase in the bleeding time from mouse tail and clot formation time. Thus, inclusion of low molecular weight anticoagulants Ado and IW into nanomaterials may be considered a way to increase their biological activity.
众所周知,通过静脉注射或经胃肠道给药进入生物体的药物会被体内的酶降解,从而降低其治疗效果。减少这一不良过程的方法之一是将药物包裹在纳米材料中。此前已证明二肽异亮氨酸-色氨酸(IW)和腺苷(Ado)具有较强的抗凝活性。在这项工作中,研究了包裹在纳米材料中对IW和Ado生物活性的影响。为此,将Ado和IW掺入由普朗尼克P123接枝肝素组成的热敏纳米凝胶中。通过透射电子显微镜、动态光散射和ζ电位对制备的纳米载体进行了表征。通过测量小鼠尾巴在体内的出血时间和体外的凝血时间来确定生物活性。发现将Ado和IW包裹在纳米材料中显著增强了它们的效果,导致小鼠尾巴出血时间和凝血时间增加。因此,将低分子量抗凝剂Ado和IW包裹在纳米材料中可被视为提高其生物活性的一种方法。