Biotin/Folate‐decorated Human Serum Albumin Nanoparticles of Docetaxel: Comparison of Chemically Conjugated Nanostructures and Physically Loaded Nanoparticles for Targeting of Breast Cancer

Navid Nateghian, Navid Goodarzi, Mohsen Amini, Fatemeh Atyabi, Mohammad Reza Khorramizadeh, Rassoul Dinarvand

Docetaxel (DTX) is a widely used chemotherapeutic agent with very low water solubility. Conjugation of DTX to Human Serum Albumin (HSA) is an effective way to increase its water solubility. Attachment of Folic Acid (FA) or biotin as targeting moieties to DTX-HSA conjugates may lead to active targeting and specific uptake by cancer cells with overexpressed FA or Biotin receptors. In this study, FA or Biotin molecules were attached to DTX-HSA conjugates by two different methods. In one method FA or Biotin molecules were attached to remaining NH2 residues of HSA in DTX-HSA conjugate by covalent bonds. In the second method HSA-FA or HSA-Biotin conjugates were synthesized separately and then combined by DTX-HSA conjugate in proper ratio to prepare nanoparticles containing DTX-HSA plus HSA-FA or HSA-Biotin. Cell viability of different nanoparticle were evaluated on MDA-MB-231 (folate receptor positive), A549 (folate receptor negative) and 4T1 (biotin receptor positive) and showed superior cytotoxicity compared with free docetaxel (Taxotere(®) ). In vivo studies of DTX-HSA-FA and DTX-HSA-Biotin conjugates in BULB/c mice, tumorized by 4T1 cell line, showed the conjugates prepared in this study were more powerful in the reduction of tumor size and increasing the survival rate when compared to free docetaxel. This article is protected by copyright. All rights reserved.