On-chip synthesis of fine-tuned bone-seeking hybrid nanoparticles

Author:

Hasani-Sadrabadi Mohammad Mahdi123,Dashtimoghadam Erfan4,Bahlakeh Ghasem5,Majedi Fatemeh S36,Keshvari Hamid3,Van Dersarl Jules J2,Bertsch Arnaud2,Panahifar Arash7,Renaud Philippe2,Tayebi Lobat48,Mahmoudi Morteza910,Jacob Karl I1

Affiliation:

1. Parker H Petit Institute for Bioengineering & Bioscience, GW Woodruff School of Mechanical Engineering & School of Materials Science & Engineering, Georgia Institute of Technology, Atlanta, GA 30332-0295, USA

2. Laboratoire de Microsystemes (LMIS4), Institute of Microengineering & Institute of Bioengineering, École Polytechnique Fédérale de Lausanne (EPFL), CH-1015 Lausanne, Switzerland

3. Department of Biomedical Engineering, Amirkabir University of Technology, Tehran, Iran

4. Department of Developmental Sciences, Marquette University School of Dentistry, Milwaukee, WI 53201, USA

5. Department of Engineering & Technology, Golestan University, AliabadKatool, Iran

6. Department of Bioengineering, University of California at Los Angeles, Los Angeles, CA 951600, USA

7. Faculty of Pharmacy & Pharmaceutical Sciences, University of Alberta, Edmonton, Alberta, Canada

8. Department of Engineering Science, University of Oxford, Oxford OX1 3PJ, UK

9. Nanotechnology Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

10. Division of Cardiovascular Medicine, School of Medicine, Stanford University, Stanford, CA 94305, USA

Abstract

Aims: Here we report a one-step approach for reproducible synthesis of finely tuned targeting multifunctional hybrid nanoparticles (HNPs). Materials & methods: A microfluidic-assisted method was employed for controlled nanoprecipitation of bisphosphonate-conjugated poly(D,L-lactide-co-glycolide) chains, while coencapsulating superparamagnetic iron oxide nanoparticles and the anticancer drug Paclitaxel. Results: Smaller and more compact HNPs with narrower size distribution and higher drug loading were obtained at microfluidic rapid mixing regimen compared with the conventional bulk method. The HNPs were shown to have a strong affinity for hydroxyapatite, as demonstrated in vitro bone-binding assay, which was further supported by molecular dynamics simulation results. In vivo proof of concept study verified the prolonged circulation of targeted microfluidic HNPs. Biodistribution as well as noninvasive bioimaging experiments showed high tumor localization and suppression of targeted HNPs to the bone metastatic tumor. Conclusion: The hybrid bone-targeting nanoparticles with adjustable characteristics can be considered as promising nanoplatforms for various theragnostic applications.

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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