-
Something wrong with this record ?
4-aminobenzoic acid-coated maghemite nanoparticles as potential anticancer drug magnetic carriers: a case study on highly cytotoxic Cisplatin-like complexes involving 7-azaindoles
P. Starha, M. Stavárek, J. Tuček, Z. Trávníček,
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Directory of Open Access Journals
from 1997
Free Medical Journals
from 1997
PubMed Central
from 2001
Europe PubMed Central
from 2001
ProQuest Central
from 1997-01-01
Open Access Digital Library
from 1997-01-01
Medline Complete (EBSCOhost)
from 2009-03-01
Health & Medicine (ProQuest)
from 1997-01-01
- MeSH
- Cisplatin administration & dosage chemistry MeSH
- Indoles chemical synthesis chemistry MeSH
- 4-Aminobenzoic Acid administration & dosage chemical synthesis chemistry MeSH
- Drug Delivery Systems * MeSH
- Humans MeSH
- Neoplasms drug therapy MeSH
- Nanoparticles chemistry MeSH
- Drug Carriers chemical synthesis chemistry MeSH
- Antineoplastic Agents chemistry MeSH
- Silver chemistry MeSH
- Ferric Compounds chemical synthesis chemistry MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
This study describes a one-pot synthesis of superparamagnetic maghemite-based 4-aminobenzoic acid-coated spherical core-shell nanoparticles (PABA@FeNPs) as suitable nanocomposites potentially usable as magnetic carriers for drug delivery. The PABA@FeNPs system was subsequently functionalized by the activated species (1* and 2*) of highly in vitro cytotoxic cis-[PtCl2(3Claza)2] (1; 3Claza stands for 3-chloro-7-azaindole) or cis-[PtCl2(5Braza)2] (2; 5Braza stands for 5-bromo-7-azaindole), which were prepared by a silver(I) ion assisted dechlorination of the parent dichlorido complexes. The products 1*@PABA@FeNPs and 2*@PABA@FeNPs, as well as an intermediate PABA@FeNPs, were characterized by a combination of various techniques, such as Mössbauer, FTIR and EDS spectroscopy, thermal analysis, SEM and TEM. The results showed that the products consist of well-dispersed maghemite-based nanoparticles of 13 nm average size that represent an easily obtainable system for delivery of highly cytotoxic cisplatin-like complexes in oncological practice.
References provided by Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14074302
- 003
- CZ-PrNML
- 005
- 20141006125103.0
- 007
- ta
- 008
- 141006s2014 sz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.3390/molecules19021622 $2 doi
- 035 __
- $a (PubMed)24476602
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a sz
- 100 1_
- $a Starha, Pavel $u Regional Centre of Advanced Technologies and Materials, Department of Inorganic Chemistry, Faculty of Science, Palacký University, 17. listopadu 12, Olomouc CZ 77146, Czech Republic. pavel.starha@upol.cz.
- 245 10
- $a 4-aminobenzoic acid-coated maghemite nanoparticles as potential anticancer drug magnetic carriers: a case study on highly cytotoxic Cisplatin-like complexes involving 7-azaindoles / $c P. Starha, M. Stavárek, J. Tuček, Z. Trávníček,
- 520 9_
- $a This study describes a one-pot synthesis of superparamagnetic maghemite-based 4-aminobenzoic acid-coated spherical core-shell nanoparticles (PABA@FeNPs) as suitable nanocomposites potentially usable as magnetic carriers for drug delivery. The PABA@FeNPs system was subsequently functionalized by the activated species (1* and 2*) of highly in vitro cytotoxic cis-[PtCl2(3Claza)2] (1; 3Claza stands for 3-chloro-7-azaindole) or cis-[PtCl2(5Braza)2] (2; 5Braza stands for 5-bromo-7-azaindole), which were prepared by a silver(I) ion assisted dechlorination of the parent dichlorido complexes. The products 1*@PABA@FeNPs and 2*@PABA@FeNPs, as well as an intermediate PABA@FeNPs, were characterized by a combination of various techniques, such as Mössbauer, FTIR and EDS spectroscopy, thermal analysis, SEM and TEM. The results showed that the products consist of well-dispersed maghemite-based nanoparticles of 13 nm average size that represent an easily obtainable system for delivery of highly cytotoxic cisplatin-like complexes in oncological practice.
- 650 _2
- $a kyselina 4-aminobenzoová $x aplikace a dávkování $x chemická syntéza $x chemie $7 D010129
- 650 _2
- $a protinádorové látky $x chemie $7 D000970
- 650 _2
- $a cisplatina $x aplikace a dávkování $x chemie $7 D002945
- 650 _2
- $a nosiče léků $x chemická syntéza $x chemie $7 D004337
- 650 12
- $a lékové transportní systémy $7 D016503
- 650 _2
- $a železité sloučeniny $x chemická syntéza $x chemie $7 D005290
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a indoly $x chemická syntéza $x chemie $7 D007211
- 650 _2
- $a nanočástice $x chemie $7 D053758
- 650 _2
- $a nádory $x farmakoterapie $7 D009369
- 650 _2
- $a stříbro $x chemie $7 D012834
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Stavárek, Martin $u Regional Centre of Advanced Technologies and Materials, Department of Inorganic Chemistry, Faculty of Science, Palacký University, 17. listopadu 12, Olomouc CZ 77146, Czech Republic. martin.stavarek01@upol.cz.
- 700 1_
- $a Tuček, Jiří $u Regional Centre of Advanced Technologies and Materials, Department of Experimental Physics, Faculty of Science, Palacký University, 17. listopadu 12, Olomouc CZ 77146, Czech Republic. jiri.tucek@upol.cz.
- 700 1_
- $a Trávníček, Zdeněk $u Regional Centre of Advanced Technologies and Materials, Department of Inorganic Chemistry, Faculty of Science, Palacký University, 17. listopadu 12, Olomouc CZ 77146, Czech Republic. zdenek.travnicek@upol.cz.
- 773 0_
- $w MED00180394 $t Molecules (Basel, Switzerland) $x 1420-3049 $g Roč. 19, č. 2 (2014), s. 1622-34
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24476602 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20141006 $b ABA008
- 991 __
- $a 20141006125540 $b ABA008
- 999 __
- $a ok $b bmc $g 1042185 $s 873214
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2014 $b 19 $c 2 $d 1622-34 $i 1420-3049 $m Molecules $n Molecules $x MED00180394
- LZP __
- $a Pubmed-20141006