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      Zerumbone-incorporated liquid crystalline nanoparticles inhibit proliferation and migration of non-small-cell lung cancer in vitro

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          Abstract

          Lung cancer is the second most prevalent type of cancer and is responsible for the highest number of cancer-related deaths worldwide. Non-small-cell lung cancer (NSCLC) makes up the majority of lung cancer cases. Zerumbone (ZER) is natural compound commonly found in the roots of Zingiber zerumbet which has recently demonstrated anti-cancer activity in both in vitro and in vivo studies. Despite their medical benefits, ZER has low aqueous solubility, poor GI absorption and oral bioavailability that hinders its effectiveness. Liquid crystalline nanoparticles (LCNs) are novel drug delivery carrier that have tuneable characteristics to enhance and ease the delivery of bioactive compounds. This study aimed to formulate ZER-loaded LCNs and investigate their effectiveness against NSCLC in vitro using A549 lung cancer cells. ZER-LCNs, prepared in the study, inhibited the proliferation and migration of A549 cells. These inhibitory effects were superior to the effects of ZER alone at a concentration 10 times lower than that of free ZER, demonstrating a potent anti-cancer activity of ZER-LCNs. The underlying mechanisms of the anti-cancer effects by ZER-LCNs were associated with the transcriptional regulation of tumor suppressor genes P53 and PTEN, and metastasis-associated gene KRT18. The protein array data showed downregulation of several proliferation associated proteins such as AXL, HER1, PGRN, and BIRC5 and metastasis-associated proteins such as DKK1, CAPG, CTSS, CTSB, CTSD, and PLAU. This study provides evidence of potential for increasing the potency and effectiveness of ZER with LCN formulation and developing ZER-LCNs as a treatment strategy for mitigation and treatment of NSCLC.

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          Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries

          This article provides an update on the global cancer burden using the GLOBOCAN 2020 estimates of cancer incidence and mortality produced by the International Agency for Research on Cancer. Worldwide, an estimated 19.3 million new cancer cases (18.1 million excluding nonmelanoma skin cancer) and almost 10.0 million cancer deaths (9.9 million excluding nonmelanoma skin cancer) occurred in 2020. Female breast cancer has surpassed lung cancer as the most commonly diagnosed cancer, with an estimated 2.3 million new cases (11.7%), followed by lung (11.4%), colorectal (10.0 %), prostate (7.3%), and stomach (5.6%) cancers. Lung cancer remained the leading cause of cancer death, with an estimated 1.8 million deaths (18%), followed by colorectal (9.4%), liver (8.3%), stomach (7.7%), and female breast (6.9%) cancers. Overall incidence was from 2-fold to 3-fold higher in transitioned versus transitioning countries for both sexes, whereas mortality varied <2-fold for men and little for women. Death rates for female breast and cervical cancers, however, were considerably higher in transitioning versus transitioned countries (15.0 vs 12.8 per 100,000 and 12.4 vs 5.2 per 100,000, respectively). The global cancer burden is expected to be 28.4 million cases in 2040, a 47% rise from 2020, with a larger increase in transitioning (64% to 95%) versus transitioned (32% to 56%) countries due to demographic changes, although this may be further exacerbated by increasing risk factors associated with globalization and a growing economy. Efforts to build a sustainable infrastructure for the dissemination of cancer prevention measures and provision of cancer care in transitioning countries is critical for global cancer control.
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            Impact of Particle Size and Polydispersity Index on the Clinical Applications of Lipidic Nanocarrier Systems

            Lipid-based drug delivery systems, or lipidic carriers, are being extensively employed to enhance the bioavailability of poorly-soluble drugs. They have the ability to incorporate both lipophilic and hydrophilic molecules and protecting them against degradation in vitro and in vivo. There is a number of physical attributes of lipid-based nanocarriers that determine their safety, stability, efficacy, as well as their in vitro and in vivo behaviour. These include average particle size/diameter and the polydispersity index (PDI), which is an indication of their quality with respect to the size distribution. The suitability of nanocarrier formulations for a particular route of drug administration depends on their average diameter, PDI and size stability, among other parameters. Controlling and validating these parameters are of key importance for the effective clinical applications of nanocarrier formulations. This review highlights the significance of size and PDI in the successful design, formulation and development of nanosystems for pharmaceutical, nutraceutical and other applications. Liposomes, nanoliposomes, vesicular phospholipid gels, solid lipid nanoparticles, transfersomes and tocosomes are presented as frequently-used lipidic drug carriers. The advantages and limitations of a range of available analytical techniques used to characterize lipidic nanocarrier formulations are also covered.
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              Solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLC) in cosmetic and dermatological preparations.

              Solid lipid nanoparticles (SLN) were developed at the beginning of the 1990 s as an alternative carrier system to emulsions, liposomes and polymeric nanoparticles. The paper reviews advantages-also potential limitations-of SLN for the use in topical cosmetic and pharmaceutical formulations. Features discussed include stabilisation of incorporated compounds, controlled release, occlusivity, film formation on skin including in vivo effects on the skin. As a novel type of lipid nanoparticles with solid matrix, the nanostructured lipid carriers (NLC) are presented, the structural specialties described and improvements discussed, for example, increase in loading capacity, physical and chemical long-term stability, triggered release and potentially supersaturated topical formulations. For both SLN and NLC, the technologies to produce the final topical formulation are described, especially the production of highly concentrated lipid nanoparticle dispersions >30-80% lipid content. Production issues also include clinical batch production, large scale production and regulatory aspects (e. g. status of excipients or proof of physical stability).
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                Author and article information

                Contributors
                dinesh_kumar@imu.edu.my
                philip.hansbro@uts.edu.au
                kamal.dua@uts.edu.au
                Journal
                Naunyn Schmiedebergs Arch Pharmacol
                Naunyn Schmiedebergs Arch Pharmacol
                Naunyn-Schmiedeberg's Archives of Pharmacology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                0028-1298
                1432-1912
                13 July 2023
                13 July 2023
                2024
                : 397
                : 1
                : 343-356
                Affiliations
                [1 ]Discipline of Pharmacy, Graduate School of Health, University of Technology Sydney, ( https://ror.org/03f0f6041) Sydney, NSW 2007 Australia
                [2 ]Australian Research Centre in Complementary and Integrative Medicine, Faculty of Health, University of Technology Sydney, ( https://ror.org/03f0f6041) Sydney, NSW 2007 Australia
                [3 ]Centre for Inflammation, Centenary Institute and University of Technology Sydney, Faculty of Science, School of Life Sciences, ( https://ror.org/05gvja138) Sydney, NSW 2050 Australia
                [4 ]GRID grid.411729.8, ISNI 0000 0000 8946 5787, School of Postgraduate Studies, , International Medical University (IMU), ; 57000 Kuala Lumpur, Malaysia
                [5 ]GRID grid.411729.8, ISNI 0000 0000 8946 5787, Department of Pharmaceutical Technology, School of Pharmacy, , International Medical University, ; 57000 Kuala Lumpur, Malaysia
                [6 ]Departamento de Química Orgánica, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, ( https://ror.org/04teye511) Av. Vicuña Mackenna 4860, 7820436 Macul, Santiago Chile
                [7 ]Centro de Investigación en Nanotecnología y Materiales Avanzados, CIEN-UC, Pontificia Universidad Católica de Chile, ( https://ror.org/04teye511) Av. Vicuña Mackenna 4860, 7820436 Macul, Santiago Chile
                [8 ]Institute for Biological and Medical Engineering, Schools of Engineering, Medicine and Biological Sciences, Pontificia Universidad Católica de Chile, ( https://ror.org/04teye511) Santiago, Chile
                [9 ]School of Biomedical Engineering, University of Technology Sydney, ( https://ror.org/03f0f6041) Sydney, New South Wales Australia
                [10 ]Institute for Biomedical Materials and Devices, Faculty of Science, University of Technology Sydney, ( https://ror.org/03f0f6041) Sydney, New South Wales Australia
                [11 ]Research and Development, Aerogen Limited, IDA Business Park, Galway, Connacht, H91 HE94 Ireland
                [12 ]School of Pharmacy & Biomolecular Sciences, Royal College of Surgeons in Ireland, ( https://ror.org/01hxy9878) Dublin, Leinster, D02 YN77 Ireland
                [13 ]School of Pharmacy & Pharmaceutical Sciences, Trinity College, ( https://ror.org/02tyrky19) Dublin, Leinster, D02 PN40 Ireland
                [14 ]Woolcock Institute of Medical Research, Macquarie University, Sydney, NSW 2137 Australia
                [15 ]School of Life Sciences, Faculty of Science, University of Technology Sydney, ( https://ror.org/03f0f6041) Sydney, NSW 2007 Australia
                [16 ]School of Pharmacy, Suresh Gyan Vihar University, ( https://ror.org/048q3sh29) Jaipur, Rajasthan India
                [17 ]Center for Transdisciplinary Research, Saveetha Institute of Medical and Technical Science, Saveetha University, ( https://ror.org/0034me914) Chennai, India
                [18 ]School of Pharmaceutical Sciences, Lovely Professional University, ( https://ror.org/00et6q107) Jalandhar-Delhi G.T Road, Phagwara, 144411 India
                [19 ]GRID grid.411729.8, ISNI 0000 0000 8946 5787, Department of Life Sciences, School of Pharmacy, , International Medical University, ; 57000 Kuala Lumpur, Malaysia
                Article
                2603
                10.1007/s00210-023-02603-5
                10771618
                37439806
                e02166cc-d3aa-44ea-8f7f-2ed06f3cf837
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 May 2023
                : 25 June 2023
                Funding
                Funded by: University of Technology Sydney
                Categories
                Research
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2024

                Pharmacology & Pharmaceutical medicine
                zerumbone,liquid crystalline nanoparticles,non-small-cell lung cancer,a549 lung cancer cells,cell proliferation,cell migration

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