2017
DOI: 10.1080/21691401.2017.1313267
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RAGE receptor targeted bioconjuguate lipid nanoparticles of diallyl disulfide for improved apoptotic activity in triple negative breast cancer: in vitro studies

Abstract: In the present study, we have demonstrated receptor for advanced glycation endproducts (RAGE) as a target for delivery of drugs specifically to triple negative breast cancer cells. We have prepared solid lipid nanoparticle formulation of cytotoxic agent di-allyl-disulfide (DADS) to overcome its bioavailability issues. Then, we have surface modified DADS-loaded solid lipid nanoparticles (DADS-SLN) with RAGE antibody to achieve site-specific delivery of DADS to TNBC cells. We found a significant cellular interna… Show more

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Cited by 51 publications
(41 citation statements)
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“…They can passively accumulate at the tumour site owing to the leaky vasculature of tumour [25]. In addition, active targeting by surface modification of suitable ligands for tumour biomarkers improves the site specificity of nanocarriers [26][27][28]. Therefore, nanocarriers are being widely employed in recent years for tumour targeted drug delivery.…”
Section: Targeting Bcscs Using Nanocarriersmentioning
confidence: 99%
“…They can passively accumulate at the tumour site owing to the leaky vasculature of tumour [25]. In addition, active targeting by surface modification of suitable ligands for tumour biomarkers improves the site specificity of nanocarriers [26][27][28]. Therefore, nanocarriers are being widely employed in recent years for tumour targeted drug delivery.…”
Section: Targeting Bcscs Using Nanocarriersmentioning
confidence: 99%
“…Among them, APAF1 plays a key role in the mechanism of apoptosis and can activate the caspase cascade reaction responsible for the apoptotic effector phase [70]. In addition, IL-10 in serum induces apoptosis of T cells by activating the caspase-8 pathway by Fas signaling [71]. New research confirms that receptor for advanced glycation endproduct (RAGE) can specifically deliver DADS into three negative breast cancer cells and significantly enhance the cytotoxicity of DADS by reducing anti-apoptotic proteins and upregulation of pro-apoptotic protein [72].…”
Section: Activation Of the Apoptotic Pathways By Dadsmentioning
confidence: 99%
“…One study showed that a SLN formulation of docetaxel functionalized with angiopep-2 can specifically bind to the LDL-receptor-related protein 1 (LRP1), which is overexpressed at the BBB, showing higher in vitro cytotoxicity and BBB permeability by receptor mediated endocytic processes [ 112 ]. Other studies are based on how to attaching a targeting ligand to an SLN, such as by linking a fatty acid of the NP to an amino group of the ligand [ 113 ], an amino group of a phospholipid to an acid group of the ligand [ 114 ], or an amino group of the chitosan coating to an acid group of the ligand [ 115 ]. These could lead to better brain drug delivery by the SLNs across BBB.…”
Section: Methods To Improve Slns For Brain Drug Deliverymentioning
confidence: 99%