(380v) ZnO Nanoparticles Incorporated MIL-100 for Doxorubicin Delivery | AIChE

(380v) ZnO Nanoparticles Incorporated MIL-100 for Doxorubicin Delivery

Authors 

Bhattacharjee, A. - Presenter, Indian Institute of Technology Guwahati
Purkait, M. K., Indian Institute of Technology Guwahati
Gumma, S., Indian Institute of Technology Tirupati

 

In the present study, an iron based metal organic framework (MOF)
MIL-100 and its composites were synthesised and evaluated
as potential carriers for doxorubicin hydrochloride. An iron based
MOF,  MIL-100 was synthesised at
150 °C using Trimesic acid (BTC) and iron powder. Zinc oxide (ZnO) nanopartcles,
that are bio-friendly and used in pharmaceutical
applications were chosen to prepare MOF composites. At first, ZnO was
prepared by wet chemical method using of Zn 2+  salt under reflux conditions. A series of
composite named ZnO@MIL-100 (Z@M_F) were prepared by adding these ZnO
nanoparticles (in varying mass %) to
the precursor solution of MIL-100. The composite
were characterised by X-ray diffraction, Nitrogen adsorption-desorption
isotherms and Transmission electron microscopy (TEM). 

Doxorubicin hydrochloride (DOX), an anticancer drug used in treatment of
diseases such as leukaemia, lymphoma, and carcinoma was chosen as a model drug. Initially, DOX was loaded
on different MOF composites. The DOX loading was
estimated through analysis of the solution phase by UV-Vis
spectrophotometer. The drug release experiments from these composites
loaded with DOX, were carried out in simulated
phosphate-buffered saline (PBS) solution of pH 7.4 at 37 °C. The highest DOX
loading capacity was found ~21% for Z2@M_F.
The release experiments indicate sustained and release of DOX after
incorporation of ZnO nanoparticles in the MOF structure.

Table : DOX loading details

Sr. No.

Sample

DOX loading (%)

01

MIL-100

10.8

02

Z1@M_F

13.3

03

Z2@M_F

21.2

04

Z3@M_F

20.4

                                                                                                

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