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Volume 3, Issue 4 (Suppl)

Nano Res Appl

ISSN: 2471-9838

November 07-08, 2017 Singapore

International Meeting on

Advanced Nanomaterials and Nanotechnology

Nanomaterials Meetings 2017

November 07-08, 2017

Page 29

pH-responsive Doxorubicin-loaded cockle shell-derived nanoparticles:

Release kinetics and pharmacokinetics in canine

Danmaigoro Abubakar, Gayathri, Thevi Selvarajah, Moh’d, Hezmee, Moh’d Noor, Rozi Mahmud and Md Zuki Abu Bakar

Universiti Putra Malaysia, Malaysia

N

anoparticles with stimuli-responsive release mechanism have received great interest in nanomedicine. Doxorubicin-loaded pH-

responsive nanocarriers could enable selectivity and specificity by reducing premature drug release in the plasma following

an intravenous administration. Doxorubicin-load cockleshell-derived nanoparticle (CSNP-DOX) was prepared via ball-milling

method. Apart from the analysis of CSNP drug release kinetics at pH 4.8 and 7.4, a high-performance liquid chromatography (HPLC)

bioanalytical method was developed for the detection of doxorubicin. For the pharmacokinetics of CSNP-DOX, Animal ethics

approval was sought. Six canines were divided into two groups to receive intravenous CSNP-DOX and free doxorubicin at 30 mg/

m

2

, respectively. At pre-determined time interval, blood was sampled and processed before analyzed by HPLC. The pharmacokinetic

parameters were determined based on the plasma doxorubicin concentration in the canines. An excellent bioanalytical method with

high acceptable extraction yield and linearity of 89.87% and 0.997 within the range limit of 0.25-4 µg/mL was revealed from the

method developed. At pH 7.4, 13.7% of DOX was released from CSNP-DOX after 96 hours while 52.6% of doxorubicin was recorded

in the free doxorubicin alone. However, the amount of doxorubicin released from the nanocarriers doubled in acidic condition.

CSNP-DOX increases the t

1/2

, T

max

and AUC

0-t

of doxorubicin. The plasma concentration of doxorubicin rapidly becomes lower versus

time when compared to the plasma concentration of CSNP-DOX. CSNP-DOX exhibited pH-triggered and sustained-drug release

properties. The pharmacokinetic parameters confirmed that CSNP has the ability to regulate and delay the release of doxorubicin in

blood circulation.

Biography

Danmaigoro Abubkar is currently a PhD student at Universiti Putra Malaysia. He is also a Lecturer at the Usmanu Danfodiyo

University, Nigeria at the Department of Veterinary Anatomy.

abubakar.danmaigoro@udusok.edu.ng

Danmaigoro Abubakar et al., Nano Res Appl 2017, 3:4

DOI: 10.21767/2471-9838-C1-005