Smart niosomes of temozolomide for enhancement of brain targeting

Drug delivery to the brain is challenging because of the low permeability of blood–brain barrier, and therefore, optimum concentration of chemotherapeutics in the target area specifically for glioblastoma, an aggressive brain tumor, opens a new path of research. To achieve the goal, the oral alkylat...

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Main Authors: Anindita De, Nagasamy Venkatesh, M Senthil, Bharat Kumar Reddy Sanapalli, R Shanmugham, Veera Venkata Satyanarayana Reddy Karri
Format: Article
Language:English
Published: SAGE Publishing 2018-10-01
Series:Nanobiomedicine
Online Access:https://doi.org/10.1177/1849543518805355
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spelling doaj-5d1cb60acf28488a9a264e789e91ed402020-11-25T03:09:33ZengSAGE PublishingNanobiomedicine1849-54352018-10-01510.1177/1849543518805355Smart niosomes of temozolomide for enhancement of brain targetingAnindita De0Nagasamy Venkatesh1M Senthil2Bharat Kumar Reddy Sanapalli3R Shanmugham4Veera Venkata Satyanarayana Reddy Karri5 Department of Pharmaceutics, JSS College of Pharmacy, Ootacamund, JSS Academy of Higher Education & Research, Mysuru, Karnataka, India Department of Pharmaceutics, JSS College of Pharmacy, Ootacamund, JSS Academy of Higher Education & Research, Mysuru, Karnataka, India Department of Pharmaceutics, JSS College of Pharmacy, Ootacamund, JSS Academy of Higher Education & Research, Mysuru, Karnataka, India Department of Pharmaceutics, JSS College of Pharmacy, Ootacamund, JSS Academy of Higher Education & Research, Mysuru, Karnataka, India Department of Pharmaceutical Analysis, Sree Vidyanikethan College of Pharmacy, Tirupati, Jawaharlal Nehru Technological University Ananthapur, Andhra Pradesh, India Department of Pharmaceutics, JSS College of Pharmacy, Ootacamund, JSS Academy of Higher Education & Research, Mysuru, Karnataka, IndiaDrug delivery to the brain is challenging because of the low permeability of blood–brain barrier, and therefore, optimum concentration of chemotherapeutics in the target area specifically for glioblastoma, an aggressive brain tumor, opens a new path of research. To achieve the goal, the oral alkylating agent temozolomide was incorporated into niosomes, and the surface was modified with chlorotoxin, a small 36 amino acid peptide discovered from the venom of scorpion Leiurus quinquestriatus . Active targeting using nanosized particles facilitates an increase in the accumulation of drugs in the cerebri by 3.04-folds. Temozolomide-loaded niosomes were prepared using conventional thin-film hydration method and characterized. Niosomes coated with chlorotoxin were produced with the size of 220 ± 1.45 nm with an entrapment efficiency of 79.09 ± 1.56%. Quantitative tissue distribution studies indicate enhanced permeation of the drug into the brain because of surface modification with less deposition in the highly perfused organs.https://doi.org/10.1177/1849543518805355
collection DOAJ
language English
format Article
sources DOAJ
author Anindita De
Nagasamy Venkatesh
M Senthil
Bharat Kumar Reddy Sanapalli
R Shanmugham
Veera Venkata Satyanarayana Reddy Karri
spellingShingle Anindita De
Nagasamy Venkatesh
M Senthil
Bharat Kumar Reddy Sanapalli
R Shanmugham
Veera Venkata Satyanarayana Reddy Karri
Smart niosomes of temozolomide for enhancement of brain targeting
Nanobiomedicine
author_facet Anindita De
Nagasamy Venkatesh
M Senthil
Bharat Kumar Reddy Sanapalli
R Shanmugham
Veera Venkata Satyanarayana Reddy Karri
author_sort Anindita De
title Smart niosomes of temozolomide for enhancement of brain targeting
title_short Smart niosomes of temozolomide for enhancement of brain targeting
title_full Smart niosomes of temozolomide for enhancement of brain targeting
title_fullStr Smart niosomes of temozolomide for enhancement of brain targeting
title_full_unstemmed Smart niosomes of temozolomide for enhancement of brain targeting
title_sort smart niosomes of temozolomide for enhancement of brain targeting
publisher SAGE Publishing
series Nanobiomedicine
issn 1849-5435
publishDate 2018-10-01
description Drug delivery to the brain is challenging because of the low permeability of blood–brain barrier, and therefore, optimum concentration of chemotherapeutics in the target area specifically for glioblastoma, an aggressive brain tumor, opens a new path of research. To achieve the goal, the oral alkylating agent temozolomide was incorporated into niosomes, and the surface was modified with chlorotoxin, a small 36 amino acid peptide discovered from the venom of scorpion Leiurus quinquestriatus . Active targeting using nanosized particles facilitates an increase in the accumulation of drugs in the cerebri by 3.04-folds. Temozolomide-loaded niosomes were prepared using conventional thin-film hydration method and characterized. Niosomes coated with chlorotoxin were produced with the size of 220 ± 1.45 nm with an entrapment efficiency of 79.09 ± 1.56%. Quantitative tissue distribution studies indicate enhanced permeation of the drug into the brain because of surface modification with less deposition in the highly perfused organs.
url https://doi.org/10.1177/1849543518805355
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