In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model
Cancer nanotherapeutics are progressing rapidly with innovative drug delivery systems to replace conventional delivery systems. Although, antitumor activity of zerumbone (ZER) has been reported, there has been no available information of ZER-loaded nanostructured lipid carrier (NLC) affects murine l...
| Main Authors: | , , , , , , , |
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| Format: | Conference or Workshop Item |
| Language: | English |
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UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience
2014
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| Online Access: | http://psasir.upm.edu.my/id/eprint/17228/ http://psasir.upm.edu.my/id/eprint/17228/1/ABSTRACT%20CAC%202014_2%20medic%2012.pdf |
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| author | Rahman, Heshu Sulaiman Abdullah, R. Othman, Hemn Hassan Chartrand, Max Stanley Abdul, Ahmad Bustamam Ajdari, Zahra Hosseinpour, Mahnaz Abdul Samad, Nozlena |
| author_facet | Rahman, Heshu Sulaiman Abdullah, R. Othman, Hemn Hassan Chartrand, Max Stanley Abdul, Ahmad Bustamam Ajdari, Zahra Hosseinpour, Mahnaz Abdul Samad, Nozlena |
| author_sort | Rahman, Heshu Sulaiman |
| building | UPM Institutional Repository |
| collection | Online Access |
| description | Cancer nanotherapeutics are progressing rapidly with innovative drug delivery systems to replace conventional delivery systems. Although, antitumor activity of zerumbone (ZER) has been reported, there has been no available information of ZER-loaded nanostructured lipid carrier (NLC) affects murine leukemia cells in vivo. In a previous study, ZER was incorporated into NLC by high pressure homogenization (HPH) technique. Physicochemical characterization included particle size, polydipersity index, zeta potential, pH, entrapment efficiency, loading capacity, stability study, and in vitro drug release, as well as physicochemical stability after being autoclaved and stored at 4˚C, 25˚C and 40˚C for 1 month, were examined. In this study, in vivo effects of ZER-NLC on murine leukemia WEHI-3B cells were investigated. The outcomes of histopathology, TEM and TUNEL assays of BALB/c leukemia mice revealed that the number of leukemia cells were significantly (P < 0.05) decreased in spleen tissue after four weeks of oral administration of ZER-NLC. In conclusion, NLC is suggested as a promising carrier for ZER oral delivery. |
| first_indexed | 2025-11-15T08:10:59Z |
| format | Conference or Workshop Item |
| id | upm-17228 |
| institution | Universiti Putra Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T08:10:59Z |
| publishDate | 2014 |
| publisher | UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | upm-172282016-04-26T03:53:42Z http://psasir.upm.edu.my/id/eprint/17228/ In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model Rahman, Heshu Sulaiman Abdullah, R. Othman, Hemn Hassan Chartrand, Max Stanley Abdul, Ahmad Bustamam Ajdari, Zahra Hosseinpour, Mahnaz Abdul Samad, Nozlena Cancer nanotherapeutics are progressing rapidly with innovative drug delivery systems to replace conventional delivery systems. Although, antitumor activity of zerumbone (ZER) has been reported, there has been no available information of ZER-loaded nanostructured lipid carrier (NLC) affects murine leukemia cells in vivo. In a previous study, ZER was incorporated into NLC by high pressure homogenization (HPH) technique. Physicochemical characterization included particle size, polydipersity index, zeta potential, pH, entrapment efficiency, loading capacity, stability study, and in vitro drug release, as well as physicochemical stability after being autoclaved and stored at 4˚C, 25˚C and 40˚C for 1 month, were examined. In this study, in vivo effects of ZER-NLC on murine leukemia WEHI-3B cells were investigated. The outcomes of histopathology, TEM and TUNEL assays of BALB/c leukemia mice revealed that the number of leukemia cells were significantly (P < 0.05) decreased in spleen tissue after four weeks of oral administration of ZER-NLC. In conclusion, NLC is suggested as a promising carrier for ZER oral delivery. UPM-MAKNA Cancer Research Laboratory, Institute of Bioscience 2014 Conference or Workshop Item PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/17228/1/ABSTRACT%20CAC%202014_2%20medic%2012.pdf Rahman, Heshu Sulaiman and Abdullah, R. and Othman, Hemn Hassan and Chartrand, Max Stanley and Abdul, Ahmad Bustamam and Ajdari, Zahra and Hosseinpour, Mahnaz and Abdul Samad, Nozlena (2014) In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model. In: Scientific Cancer Research Poster Competition in conjunction with Cancer Awareness Carnival 2014, 10 May 2014, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia. . |
| spellingShingle | Rahman, Heshu Sulaiman Abdullah, R. Othman, Hemn Hassan Chartrand, Max Stanley Abdul, Ahmad Bustamam Ajdari, Zahra Hosseinpour, Mahnaz Abdul Samad, Nozlena In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| title | In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| title_full | In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| title_fullStr | In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| title_full_unstemmed | In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| title_short | In vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| title_sort | in vivo assessment of nanostructured lipid carrier for oral delivery of zerumbone in leukemic mice model |
| url | http://psasir.upm.edu.my/id/eprint/17228/ http://psasir.upm.edu.my/id/eprint/17228/1/ABSTRACT%20CAC%202014_2%20medic%2012.pdf |