2016
DOI: 10.2147/ijn.s105427
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Chitosan-based nanoparticles for survivin targeted siRNA delivery in breast tumor therapy and preventing its metastasis

Abstract: Nanoparticle-mediated small interfering RNA (siRNA) delivery is a promising therapeutic strategy in various cancers. However, it is difficult to deliver degradative siRNA to tumor tissue, and thus a safe and efficient vector for siRNA delivery is essential for cancer therapy. In this study, poly(ethylene glycol)-modified chitosan (PEG-CS) was synthesized successfully for delivering nucleic acid drug. We deemed that PEGylated CS could improve its solubility by forming a stable siRNA loaded in nanoparticles, and… Show more

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Cited by 73 publications
(44 citation statements)
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“…Also, poly (ethylene glycol)modified chitosan NPs were synthesized to encapsulate and deliver small interfering RNA (siRNA). The siRNA loaded NPs showed 4T1 cell inhibition both in vitro and in vivo ensuring its efficacy in reduction of tumor growth and metastasis (Sun et al, 2016). Wan et al developed the lapatinib-loaded human serum albumin NPs that exhibited a core-shell structure with stealth properties preventing brain metastasis from triple-negative breast cancer (Wan et al, 2016).…”
Section: Breast Cancermentioning
confidence: 99%
“…Also, poly (ethylene glycol)modified chitosan NPs were synthesized to encapsulate and deliver small interfering RNA (siRNA). The siRNA loaded NPs showed 4T1 cell inhibition both in vitro and in vivo ensuring its efficacy in reduction of tumor growth and metastasis (Sun et al, 2016). Wan et al developed the lapatinib-loaded human serum albumin NPs that exhibited a core-shell structure with stealth properties preventing brain metastasis from triple-negative breast cancer (Wan et al, 2016).…”
Section: Breast Cancermentioning
confidence: 99%
“…Thus, there may be some difficulties in adhering to technologies involving siRNA because there are few firms with expertise in their development which delays the approval of drugs. It is difficult to correctly deliver siRNA treatments without the drugs being degraded by nuclease enzymes and without promoting side effects [24]. This technological challenge is also observed in treatments involving cell therapy [25].…”
Section: Clinical Trials Involving Vaccines and New Therapies For Covmentioning
confidence: 99%
“…Also, CS could be exploited as an ideal delivery carrier to protect microRNA and other noncoding RNAs from RNase to prevent their degradation and poor penetration. Indeed, related results have demonstrated that PEG‐CS nanoparticles were successfully developed to be safe and efficient vectors for siRNA delivery (Sun et al, 2016). Additionally, it has also been reported that siRNA conjugated CS nanoparticles fabricated with antibody could specifically target M1 macrophages and reduce the expression of iNOS, enhance the functional recovery by inhibiting of the apoptosis in the lesion site of injured spinal cord (Gao and Li, 2017).…”
Section: Sustained Release Of Neurotrophic Factors By Chitosan Complementioning
confidence: 99%