Molecular encapsulator on the surface of magnetic nanoparticles. Controlled drug release from calcium Ferrite/Cyclodextrin–tethered polymer hybrid

[Display omitted] •75 nm-sized calcium ferrite nanoparticles are prepared as drug delivery agents.•The β-Cyclodextrin–tethered dextran-coated nanoparticles are loaded with camptothecin.•Cytotoxicity on human cervical cancer cells is studied.•The toxicity of the nanoparticles on brine shrimp, Artemia...

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Published inColloids and surfaces, B, Biointerfaces Vol. 161; pp. 347 - 355
Main Authors Ramasamy, Sivaraj, Samathanam, Beniya, Reuther, Helfried, Adyanpuram, Muthukumar Nadar Meenakshi Subbaraman, Enoch, Israel Vijayaraj Muthu Vijayan, Potzger, Kay
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.01.2018
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Abstract [Display omitted] •75 nm-sized calcium ferrite nanoparticles are prepared as drug delivery agents.•The β-Cyclodextrin–tethered dextran-coated nanoparticles are loaded with camptothecin.•Cytotoxicity on human cervical cancer cells is studied.•The toxicity of the nanoparticles on brine shrimp, Artemia salina, is reduced on the polymer coating. Magnetic nanoparticles (MNPs) are intriguing due to their potency to deliver anti-cancer drugs. This paper presents the inference from our experimental attempts to add merit to the concept of magnetic drug carrier, by designing calcium ferrite nanoparticles and coating them with a biocompatible dextran tethered with a hydrophobic cavity-containing molecule, β-cyclodextrin (β-CD). The size, crystal system, and the morphology of the MNPs are studied. The magnetic properties are explored using vibrating sample magnetometry, SQUID and Mössbauer spectroscopy. The roughly 75nm MNPs, encapsulated with the β-CD–dextran conjugate allows a slow and sustained in vitro release of the loaded anti-cancer drug, Camptothecin, from the polymer shell. The study of cytotoxicity reveals that the loaded Camptothecin retains its potency as efficient as an effective carrier of the anti-cancer drug. Further, the toxicity of the nanomaterial is tested on an organism which is highly sensitive to toxicity i.e., brine shrimp (Artemia salina). The polymer coating brings down the toxicity of the MNPs.
AbstractList Magnetic nanoparticles (MNPs) are intriguing due to their potency to deliver anti-cancer drugs. This paper presents the inference from our experimental attempts to add merit to the concept of magnetic drug carrier, by designing calcium ferrite nanoparticles and coating them with a biocompatible dextran tethered with a hydrophobic cavity-containing molecule, β-cyclodextrin (β-CD). The size, crystal system, and the morphology of the MNPs are studied. The magnetic properties are explored using vibrating sample magnetometry, SQUID and Mössbauer spectroscopy. The roughly 75nm MNPs, encapsulated with the β-CD–dextran conjugate allows a slow and sustained in vitro release of the loaded anti-cancer drug, Camptothecin, from the polymer shell. The study of cytotoxicity reveals that the loaded Camptothecin retains its potency as efficient as an effective carrier of the anti-cancer drug. Further, the toxicity of the nanomaterial is tested on an organism which is highly sensitive to toxicity i.e., brine shrimp (Artemia salina). The polymer coating brings down the toxicity of the MNPs.
Magnetic nanoparticles (MNPs) are intriguing due to their potency to deliver anti-cancer drugs. This paper presents the inference from our experimental attempts to add merit to the concept of magnetic drug carrier, by designing calcium ferrite nanoparticles and coating them with a biocompatible dextran tethered with a hydrophobic cavity-containing molecule, β-cyclodextrin (β-CD). The size, crystal system, and the morphology of the MNPs are studied. The magnetic properties are explored using vibrating sample magnetometry, SQUID and Mössbauer spectroscopy. The roughly 75nm MNPs, encapsulated with the β-CD-dextran conjugate allows a slow and sustained in vitro release of the loaded anti-cancer drug, Camptothecin, from the polymer shell. The study of cytotoxicity reveals that the loaded Camptothecin retains its potency as efficient as an effective carrier of the anti-cancer drug. Further, the toxicity of the nanomaterial is tested on an organism which is highly sensitive to toxicity i.e., brine shrimp (Artemia salina). The polymer coating brings down the toxicity of the MNPs.Magnetic nanoparticles (MNPs) are intriguing due to their potency to deliver anti-cancer drugs. This paper presents the inference from our experimental attempts to add merit to the concept of magnetic drug carrier, by designing calcium ferrite nanoparticles and coating them with a biocompatible dextran tethered with a hydrophobic cavity-containing molecule, β-cyclodextrin (β-CD). The size, crystal system, and the morphology of the MNPs are studied. The magnetic properties are explored using vibrating sample magnetometry, SQUID and Mössbauer spectroscopy. The roughly 75nm MNPs, encapsulated with the β-CD-dextran conjugate allows a slow and sustained in vitro release of the loaded anti-cancer drug, Camptothecin, from the polymer shell. The study of cytotoxicity reveals that the loaded Camptothecin retains its potency as efficient as an effective carrier of the anti-cancer drug. Further, the toxicity of the nanomaterial is tested on an organism which is highly sensitive to toxicity i.e., brine shrimp (Artemia salina). The polymer coating brings down the toxicity of the MNPs.
[Display omitted] •75 nm-sized calcium ferrite nanoparticles are prepared as drug delivery agents.•The β-Cyclodextrin–tethered dextran-coated nanoparticles are loaded with camptothecin.•Cytotoxicity on human cervical cancer cells is studied.•The toxicity of the nanoparticles on brine shrimp, Artemia salina, is reduced on the polymer coating. Magnetic nanoparticles (MNPs) are intriguing due to their potency to deliver anti-cancer drugs. This paper presents the inference from our experimental attempts to add merit to the concept of magnetic drug carrier, by designing calcium ferrite nanoparticles and coating them with a biocompatible dextran tethered with a hydrophobic cavity-containing molecule, β-cyclodextrin (β-CD). The size, crystal system, and the morphology of the MNPs are studied. The magnetic properties are explored using vibrating sample magnetometry, SQUID and Mössbauer spectroscopy. The roughly 75nm MNPs, encapsulated with the β-CD–dextran conjugate allows a slow and sustained in vitro release of the loaded anti-cancer drug, Camptothecin, from the polymer shell. The study of cytotoxicity reveals that the loaded Camptothecin retains its potency as efficient as an effective carrier of the anti-cancer drug. Further, the toxicity of the nanomaterial is tested on an organism which is highly sensitive to toxicity i.e., brine shrimp (Artemia salina). The polymer coating brings down the toxicity of the MNPs.
Author Enoch, Israel Vijayaraj Muthu Vijayan
Samathanam, Beniya
Potzger, Kay
Ramasamy, Sivaraj
Adyanpuram, Muthukumar Nadar Meenakshi Subbaraman
Reuther, Helfried
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  givenname: Muthukumar Nadar Meenakshi Subbaraman
  surname: Adyanpuram
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  organization: Helmholtz-Zentrum Dresden-Rossendorf, Institut für Ionenstrahlphysik und Materialforschung, Abteilung Magnetismus, Bautzner Landstrasse 400, 01328, Dresden, Germany
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Keywords Surface functionalization
Drug release
Cyclodextrin
Host-guest interface
Magnetic nanoparticles
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SSID ssj0002417
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Snippet [Display omitted] •75 nm-sized calcium ferrite nanoparticles are prepared as drug delivery agents.•The β-Cyclodextrin–tethered dextran-coated nanoparticles are...
Magnetic nanoparticles (MNPs) are intriguing due to their potency to deliver anti-cancer drugs. This paper presents the inference from our experimental...
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SubjectTerms antineoplastic agents
Artemia salina
beta-cyclodextrin
calcium
coatings
colloids
Cyclodextrin
cytotoxicity
dextran
drug carriers
Drug release
ferrimagnetic materials
Host-guest interface
hydrophobicity
Magnetic nanoparticles
magnetic properties
magnetism
nanoparticles
polymers
spectroscopy
Surface functionalization
Title Molecular encapsulator on the surface of magnetic nanoparticles. Controlled drug release from calcium Ferrite/Cyclodextrin–tethered polymer hybrid
URI https://dx.doi.org/10.1016/j.colsurfb.2017.10.048
https://www.ncbi.nlm.nih.gov/pubmed/29100128
https://www.proquest.com/docview/1976010936
https://www.proquest.com/docview/2000546425
Volume 161
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