Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes

Leanne De Silva,1 Ju-Yen Fu,2 Thet Thet Htar,1 Saravanan Muniyandy,3 Azahari Kasbollah,4 Wan Hamirul Bahrin Wan Kamal,4 Lay-Hong Chuah1,5 1School of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia; 2Nutrition Unit, Malaysian Palm Oil Board, Bandar Baru Bangi, Selangor, Malay...

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Autores principales: De Silva L, Fu JY, Htar TT, Muniyandy S, Kasbollah A, Wan Kamal WHB, Chuah LH
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Publicado: Dove Medical Press 2019
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spelling oai:doaj.org-article:6c0482d3964d46bb923ff432b2bf2d302021-12-02T04:38:07ZCharacterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes1178-2013https://doaj.org/article/6c0482d3964d46bb923ff432b2bf2d302019-02-01T00:00:00Zhttps://www.dovepress.com/characterization-optimization-and-in-vitro-evaluation-of-technetium-99-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Leanne De Silva,1 Ju-Yen Fu,2 Thet Thet Htar,1 Saravanan Muniyandy,3 Azahari Kasbollah,4 Wan Hamirul Bahrin Wan Kamal,4 Lay-Hong Chuah1,5 1School of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia; 2Nutrition Unit, Malaysian Palm Oil Board, Bandar Baru Bangi, Selangor, Malaysia; 3Department of Pharmacy, Fatima College of Health Sciences, Al Ain, United Arab Emirates; 4Medical Technology Division, Malaysian Nuclear Agency, Bangi, Selangor, Malaysia; 5Advanced Engineering Platform, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia Background and purpose: Niosomes are nonionic surfactant-based vesicles that exhibit certain unique features which make them favorable nanocarriers for sustained drug delivery in cancer therapy. Biodistribution studies are critical in assessing if a nanocarrier system has preferential accumulation in a tumor by enhanced permeability and retention effect. Radiolabeling of nanocarriers with radioisotopes such as Technetium-99m (99mTc) will allow for the tracking of the nanocarrier noninvasively via nuclear imaging. The purpose of this study was to formulate, characterize, and optimize 99mTc-labeled niosomes. Methods: Niosomes were prepared from a mixture of sorbitan monostearate 60, cholesterol, and synthesized D-α-tocopherol polyethylene glycol 1000 succinate-diethylenetriaminepentaacetic acid (synthesis confirmed by 1H and 13C nuclear magnetic resonance spectroscopy). Niosomes were radiolabeled by surface chelation with reduced 99mTc. Parameters affecting the radiolabeling efficiency such as concentration of stannous chloride (SnCl2·H2O), pH, and incubation time were evaluated. In vitro stability of radiolabeled niosomes was studied in 0.9% saline and human serum at 37°C for up to 8 hours. Results: Niosomes had an average particle size of 110.2±0.7 nm, polydispersity index of 0.229±0.008, and zeta potential of -64.8±1.2 mV. Experimental data revealed that 30 µg/mL of SnCl2·H2O was the optimal concentration of reducing agent required for the radiolabeling process. The pH and incubation time required to obtain high radiolabeling efficiency was pH 5 and 15 minutes, respectively. 99mTc-labeled niosomes exhibited high radiolabeling efficiency (>90%) and showed good in vitro stability for up to 8 hours. Conclusion: To our knowledge, this is the first study published on the surface chelation of niosomes with 99mTc. The formulated 99mTc-labeled niosomes possessed high radiolabeling efficacy, good stability in vitro, and show good promise for potential use in nuclear imaging in the future. Keywords: nanotechnology, nanocarriers, radiolabeling, drug delivery, formulation, nuclear imagingDe Silva LFu JYHtar TTMuniyandy SKasbollah AWan Kamal WHBChuah LHDove Medical PressarticleNiosomesnanocarriersradiolabelingTechnetium-99mMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 14, Pp 1101-1117 (2019)
institution DOAJ
collection DOAJ
language EN
topic Niosomes
nanocarriers
radiolabeling
Technetium-99m
Medicine (General)
R5-920
spellingShingle Niosomes
nanocarriers
radiolabeling
Technetium-99m
Medicine (General)
R5-920
De Silva L
Fu JY
Htar TT
Muniyandy S
Kasbollah A
Wan Kamal WHB
Chuah LH
Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes
description Leanne De Silva,1 Ju-Yen Fu,2 Thet Thet Htar,1 Saravanan Muniyandy,3 Azahari Kasbollah,4 Wan Hamirul Bahrin Wan Kamal,4 Lay-Hong Chuah1,5 1School of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia; 2Nutrition Unit, Malaysian Palm Oil Board, Bandar Baru Bangi, Selangor, Malaysia; 3Department of Pharmacy, Fatima College of Health Sciences, Al Ain, United Arab Emirates; 4Medical Technology Division, Malaysian Nuclear Agency, Bangi, Selangor, Malaysia; 5Advanced Engineering Platform, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia Background and purpose: Niosomes are nonionic surfactant-based vesicles that exhibit certain unique features which make them favorable nanocarriers for sustained drug delivery in cancer therapy. Biodistribution studies are critical in assessing if a nanocarrier system has preferential accumulation in a tumor by enhanced permeability and retention effect. Radiolabeling of nanocarriers with radioisotopes such as Technetium-99m (99mTc) will allow for the tracking of the nanocarrier noninvasively via nuclear imaging. The purpose of this study was to formulate, characterize, and optimize 99mTc-labeled niosomes. Methods: Niosomes were prepared from a mixture of sorbitan monostearate 60, cholesterol, and synthesized D-α-tocopherol polyethylene glycol 1000 succinate-diethylenetriaminepentaacetic acid (synthesis confirmed by 1H and 13C nuclear magnetic resonance spectroscopy). Niosomes were radiolabeled by surface chelation with reduced 99mTc. Parameters affecting the radiolabeling efficiency such as concentration of stannous chloride (SnCl2·H2O), pH, and incubation time were evaluated. In vitro stability of radiolabeled niosomes was studied in 0.9% saline and human serum at 37°C for up to 8 hours. Results: Niosomes had an average particle size of 110.2±0.7 nm, polydispersity index of 0.229±0.008, and zeta potential of -64.8±1.2 mV. Experimental data revealed that 30 µg/mL of SnCl2·H2O was the optimal concentration of reducing agent required for the radiolabeling process. The pH and incubation time required to obtain high radiolabeling efficiency was pH 5 and 15 minutes, respectively. 99mTc-labeled niosomes exhibited high radiolabeling efficiency (>90%) and showed good in vitro stability for up to 8 hours. Conclusion: To our knowledge, this is the first study published on the surface chelation of niosomes with 99mTc. The formulated 99mTc-labeled niosomes possessed high radiolabeling efficacy, good stability in vitro, and show good promise for potential use in nuclear imaging in the future. Keywords: nanotechnology, nanocarriers, radiolabeling, drug delivery, formulation, nuclear imaging
format article
author De Silva L
Fu JY
Htar TT
Muniyandy S
Kasbollah A
Wan Kamal WHB
Chuah LH
author_facet De Silva L
Fu JY
Htar TT
Muniyandy S
Kasbollah A
Wan Kamal WHB
Chuah LH
author_sort De Silva L
title Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes
title_short Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes
title_full Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes
title_fullStr Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes
title_full_unstemmed Characterization, optimization, and in vitro evaluation of Technetium-99m-labeled niosomes
title_sort characterization, optimization, and in vitro evaluation of technetium-99m-labeled niosomes
publisher Dove Medical Press
publishDate 2019
url https://doaj.org/article/6c0482d3964d46bb923ff432b2bf2d30
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