Essential oil loaded pectin/chitosan nanoparticles preparation and optimization via Box-Behnken design against MCF-7 breast cancer cell lines

被引:53
作者
Attallah, Olivia A. [1 ,2 ]
Shetta, Amro [1 ]
Elshishiny, Fatma [1 ]
Mamdouh, Wael [1 ]
机构
[1] Amer Univ Cairo, Sch Sci & Engn, Dept Chem, AUC Ave,POB 74, New Cairo 11835, Egypt
[2] Heliopolis Univ, Fac Pharm, Pharmaceut Chem Dept, Cairo Belbeis Desert Rd, Cairo 11777, Egypt
关键词
AROMATHERAPY MASSAGE; PECTIN; CHITOSAN; EFFICACY;
D O I
10.1039/c9ra10204c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the continuous search for effective cancer treatments, we here report a novel anticancer nanoparticulate system composed of jasmine oil (JO), an essential oil with proven anticancer activity and pectin/chitosan composite nanoparticles (Pec/CS NPs) as encapsulating materials to overcome JO's solubility and sensitivity problems using a green ionotropic gelation method. Pec/CS/JO NPs were formulated using Box-Behnken design (BBD) to estimate the interactions and effects of studied formulation variables on particle size, zeta potential and encapsulation efficiency to develop an optimized Pec/CS nanoformulation. The nano-encapsulation system preserved the consistency of total phenolic contents in JO and amended its thermal stability by 1.64 fold. The antioxidant potency of JO was enhanced after encapsulation by 96.28%. Consequently, the cytotoxic activity of bare Pec/CS NPs, pure JO and encapsulated JO in Pec/CS NPs against (MCF-7) breast cancer cells and (L-929) normal cells was evaluated using MTT assay. Encapsulated JO was more potent than pure JO with approximate to 13 fold improvement in anticancer activity, whereas the cell viability of normal cells wasn't affected but was rather enhanced when treated with Pec/CS NPs.
引用
收藏
页码:8703 / 8708
页数:6
相关论文
共 26 条
[1]   Transforming large molecular weight pectin and chitosan into oral protein drug nanoparticulate carrier [J].
Al-Azi, Syed Othman Syed Mohamad ;
Tan, Yvonne Tze Fung ;
Wong, Tin Wui .
REACTIVE & FUNCTIONAL POLYMERS, 2014, 84 :45-52
[2]   Characterization of Self-Assembled Polyelectrolyte Complex Nanoparticles Formed from Chitosan and Pectin [J].
Birch, Nathan P. ;
Schiffman, Jessica D. .
LANGMUIR, 2014, 30 (12) :3441-3447
[3]   An Integrin-Targeting RGDK-Tagged Nanocarrier: Anticancer Efficacy of Loaded Curcumin [J].
Das, Krishnendu ;
Nimushakavi, Sahithi ;
Chaudhuri, Arabinda ;
Das, Prasanta Kumar .
CHEMMEDCHEM, 2017, 12 (10) :738-750
[4]   Core-Shell Silver/Polymeric Nanoparticles-Based Combinatorial Therapy against Breast Cancer In-vitro [J].
Elbaz, Nancy M. ;
Ziko, Laila ;
Siam, Rania ;
Mamdouh, Wael .
SCIENTIFIC REPORTS, 2016, 6
[5]  
Elisha E. E., 1988, PHARM BIOL, V26, P221
[6]  
Fahrurroji A, 2017, INT J PHARM PHARM SC, V9, P98, DOI DOI 10.22159/ijpps.2017v9i12.19816
[7]   Physicochemical characterization of protein-loaded pectin-chitosan nanoparticles prepared by polyelectrolyte complexation [J].
Grabnar, P. Ahlin ;
Kristl, J. .
PHARMAZIE, 2010, 65 (11) :851-852
[8]  
Hongratanaworakit T, 2010, NAT PROD COMMUN, V5, P157
[9]   Aromatherapy massage affects menopausal symptoms in Korean climacteric women: A pilot-controlled clinical trial [J].
Hur, Myung-Haeng ;
Yang, Yun Seok ;
Lee, Myeong Soo .
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE, 2008, 5 (03) :325-328
[10]   Preparation of Ionically Cross-Linked Pectin Nanoparticles in the Presence of Chlorides of Divalent and Monovalent Cations [J].
Jonassen, Helene ;
Treves, Alessandro ;
Kjoniksen, Anna-Lena ;
Smistad, Gro ;
Hiorth, Marianne .
BIOMACROMOLECULES, 2013, 14 (10) :3523-3531