Title of article :
Caffeic Acid Phenethyl Ester Loaded Poly (ε -caprolactone) Nanoparticles for Improved Anticancer Efficacy: Formulation Development, Characterization and in Vitro Cytotoxicity Study
Author/Authors :
Kapare, Harshad S Department of Quality Assurance Techniques - Poona College of Pharmacy - Bharati Vidyapeeth University - Erandwane - Pune - India , Sathiyanarayanan, Lohidasan Department of Pharmaceutical Chemistry - Poona College of Pharmacy - Bharati Vidyapeeth University - Erandwane - Pune - India , S, Arulmozhi Department of Pharmacology - Poona College of Pharmacy - Bharati Vidyapeeth University - Erandwane - Pune - India , Mahadik, Kakasaheb R Department of Pharmaceutical Chemistry - Poona College of Pharmacy - Bharati Vidyapeeth University - Erandwane - Pune - India
Abstract :
Cytotoxic potential of caffeic acid phenethyl ester (CAPE) which is an active
constituent of bee propolis is well proven. The therapeutic efficacy of CAPE is
affected due to poor solubility and bioavailability. In present study CAPE loaded
Poly (ε-caprolactone) nanoparticles formulation (denoted as CPL) was designed
and investigated with the aims of enhancement of solubility, anticancer
efficacy and to achieve desired characteristics. Design of experiment approach
is implemented in formulation development. Developed formulations were
evaluated in detail for nanoparticle characterization and in vitro cytotoxicity
study. Developed nanoparticles showed particle size and encapsulation
efficiency of 187 ± 2 - 220 ± 2 nm and 64.37+ 1.20- 74.80+ 1.45% respectively.
Desirable characteristics in terms of drug content, in vitro release, surface
morphology were observed. Total growth inhibition concentration was observed
to be decreased by 40.87% for developed formulation as compared to CAPE in
MCF-7 cells and 23.73% in human colon cancer cells HT-29. The study proven
that the developed CPL exhibited improved solubility, sustained drug release,
enhanced in vitro cytotoxicity in MCF-7 and HT-29 cell lines in comparison with
pure CAPE. Thus the proposed system may be served as a useful tool for cancer
treatment.
Keywords :
Design of experiment , Sulforhodamine B (SRB) , Assay , Nanotechnology , Anticancer
Journal title :
Nanomedicine Research Journal