Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, United States; Koch Institute of Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, United States; Institute for Soldier Nanotechnologies, Massachusetts Institute of Technology, Cambridge, MA 02139, United States; Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139, United States.
Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, United States; Koch Institute of Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, United States.
J Control Release. 2017 Sep 28;262:1-9. doi: 10.1016/j.jconrel.2017.07.003. Epub 2017 Jul 6.
All-trans retinoic acid (ATRA), a derivative of vitamin A, is a common component in cosmetics and commercial acne creams as well as being a first-line chemotherapeutic agent. Today, formulations for the topical application of ATRA rely on creams and emulsions to incorporate the highly hydrophobic ATRA drug. These strategies, when applied to the skin, deliver ATRA as a single bolus, which is immediately taken up into the skin and contributes to many of the known adverse side effects of ATRA treatment, including skin irritation and hair loss. Herein we present a new concept in topical delivery of retinoids by covalently bonding the drug through a hydrolytically degradable ester linkage to a common hydrophilic polymer, polyvinyl alcohol (PVA), creating an amphiphilic nanomaterial that is water-soluble. This PVA bound ATRA can then act as a pro-drug and accumulate within the skin to allow for the sustained controlled delivery of active ATRA. This approach was demonstrated to release active ATRA out to 10days in vitro while significantly enhancing dermal accumulation of the ATRA in explant pig skin. In vivo we demonstrate that the pro-drug formulation reduces application site inflammation compared to free ATRA and retains the drug at the application site at measurable quantities for up to six days.
全反式视黄酸(ATRA)是维生素 A 的一种衍生物,是化妆品和商业痤疮霜中的常见成分,也是一线化疗药物。如今,用于局部应用 ATRA 的制剂依赖于乳膏和乳液来掺入高度疏水的 ATRA 药物。这些策略在应用于皮肤时,将 ATRA 作为单次推注给药,这会立即被皮肤吸收,并导致 ATRA 治疗的许多已知不良反应,包括皮肤刺激和脱发。在此,我们通过将药物通过可水解的酯键共价键合到常见的亲水性聚合物聚乙烯醇(PVA)上来呈现一种新型的视黄醇类药物的局部传递概念,从而形成一种具有两亲性的纳米材料,水溶性的。这种与 PVA 结合的 ATRA 可以作为前药,在皮肤内积累,从而允许持续控制 ATRA 的活性释放。该方法在体外被证明可以释放出 10 天的活性 ATRA,同时显著增加离体猪皮中 ATRA 的真皮积累。在体内,我们证明与游离 ATRA 相比,前药制剂可减少给药部位的炎症,并可在长达六天的时间内以可测量的量将药物保留在给药部位。