2019
DOI: 10.1111/ijac.13231
|View full text |Cite
|
Sign up to set email alerts
|

Hybrid polymeric systems of mesoporous silica/hydroxyapatite nanoparticles applied as antitumor drug delivery platform

Abstract: In this study, we report the production of a mesoporous silica/hydroxyapatite‐based nanocomposite containing copper (Cu) functionalized with methacrylic acid (MAA), a pH‐sensitive polymer. The functionalization of the nanoparticles surface was performed using the microwave method in order to anchor the cross‐linking tetraethylene glycol dimethacrylate (TEGDMA), onto the nanoparticles surface followed by MAA polymerization. The materials were characterized by XRD, XRF spectroscopy, scanning and transmission ele… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
5

Citation Types

0
15
0

Year Published

2020
2020
2023
2023

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 17 publications
(17 citation statements)
references
References 49 publications
0
15
0
Order By: Relevance
“…The drug delivery from hydroxyapatite minimizes the toxicity to other organs reducing the drug concentration in the blood, avoiding repeated dosage of drugs. HAP easily binds to both positive and negative molecules by simple adsorption and is used for delivery of molecules like antibiotics, contraceptives, acetylsalicylic acid, hormones, insulin and anticancer drugs [26][27][28]. The HAP doping/substitution with different kind of elements (Mg, Si, Sr, Eu, Zn, Ce) was proposed as a way to improve the drug loading [29][30][31].…”
Section: Introductionmentioning
confidence: 99%
“…The drug delivery from hydroxyapatite minimizes the toxicity to other organs reducing the drug concentration in the blood, avoiding repeated dosage of drugs. HAP easily binds to both positive and negative molecules by simple adsorption and is used for delivery of molecules like antibiotics, contraceptives, acetylsalicylic acid, hormones, insulin and anticancer drugs [26][27][28]. The HAP doping/substitution with different kind of elements (Mg, Si, Sr, Eu, Zn, Ce) was proposed as a way to improve the drug loading [29][30][31].…”
Section: Introductionmentioning
confidence: 99%
“…The first is the use of HAp scaffolds as drug delivery composites. Associated with anti-tumor drugs, such as doxorubicin, cisplatin, and methotrexate (27)(28)(29)(30)(31)(32), the gradual detachment of these molecules in specific places is guaranteed, also allowing the optimal in loco concentration Abbreviations: ADM, Adriamycin; AMPK, Adenylate-activated protein kinase; FeHA, iron-doped hydroxyapatite; HAp, Hydroxyapatite; hBMSCs, human bone mesenchymal stem cells; HeLa cells, cellular lineage commonly used in studies to assess cell proliferation, cytotoxicity and mortality; HepG2, liver cancer cell line (HepG2); INCA, National Cancer Institute; IOHAp, iron oxide (Fe 2 O 3 ) nanoparticles coated with HAp; K7M2-pCl, including osteosarcoma cells (K7M2-pCl); LbL1, one layer-layer-by-layer scaffold produced from collagen, HAp, magnetite and cisplatin; LbL3, three-layer-layer-by-layer scaffold produced from collagen, HAp, magnetite and cisplatin; LbL5, five layer-layer-by-layer scaffold produced from collagen, HAp, magnetite and cisplatin; LbL7, seven-layerlayer-by-layer scaffold produced from collagen, HAp, magnetite and cisplatin; Mag@CaP, iron oxide nanoparticles coated with amorphous calcium phosphate; MC3T3-E1, Cellular adhesion and proliferation potential of the osteoblastic cell line MC3T3-E1; MG-63, human osteosarcoma lineage cells (MG-63); MH, magnetic hyperthermia; MNPs, magnetic nanoparticles; MRI, magnetic resonance imaging; FeHApC, nanohydroxyapatite/collagen; PCR, polymerase chain reaction; PLGA, poly(lactic-co-glycolic acid); Saos-2, human osteosarcoma cellular lineage (Saos-2). of the respective drug, which is sustained for more extended periods, thus avoiding undesirable side effects (33)(34)(35)(36).…”
Section: Introductionmentioning
confidence: 99%
“…The first is the use of HAp scaffolds as drug delivery composites. Associated with anti-tumor drugs, such as doxorubicin, cisplatin, and methotrexate ( 27 32 ), the gradual detachment of these molecules in specific places is guaranteed, also allowing the optimal in loco concentration of the respective drug, which is sustained for more extended periods, thus avoiding undesirable side effects ( 33 36 ). The second research front focuses on associating HAp with magnetic nanoparticles (MNPs), to guarantee their biocompatibility ( 37 ).…”
Section: Introductionmentioning
confidence: 99%
“…HAp exhibits excellent biocompatibility and bioresorbability [ 15 ]. Thus, various DDS carriers using HAp have been reported [ 16 , 17 , 18 , 19 , 20 ]. Tetracycline hydrochloride, an antibiotic, loaded onto porous HAp was composited with polycaprolactone, and the drug-release behavior of the composite was controlled by varying the mixing ratio [ 16 ].…”
Section: Introductionmentioning
confidence: 99%