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Table 7 Nanogel based anti-GBM drug delivery system

From: Nanoscale Drug Delivery Systems in Glioblastoma

Drug

Composite

Modification

Detail

Result

Teriflunomide (TFM) [188]

TFM@ Gellan gum@ Carbopol 974P

Gellan gum and carbopol 974P were applied as gelling and mucoadhesive agents

Ex vivo nasal permeation was performed by using vertical Franz diffusion cell

Cellular uptake, bio-distribution and proliferation were evaluated in U87MG cells

Systematic toxicity and bio-distribution were determined in Swiss albino mice model

Enhanced nasal permeation and brain accumulation through i.n. delivery

High cytotoxicity potential against tumor cells

No hepatotoxicity, nephrotoxicity and hematological toxicity

Doxorubicin [189]

DOX@Lf@PBA@HA

Lactoferrin was coated onto the nanogels to achive blood brain barrier penetration

Hyaluronic acid and phenylboronic acid provided dual targeting for tumor

Cellular uptake and disposition were determined through flow cytometry and CLMS

B.End3/G422 coculture model was used to study the transport ability

SD rats and ICR mice were utilized to investigate anti-tumor efficacy and bio-distribution respectively

Triggered drug release manner by high GSH

Increased cellular uptake through clathrin and caveolin-mediated endocytosis

Optimized bio-distribution and higher permeation ability

TSPO ligand [190]

TSPO ligand-DEX@NG

Cholesterol and porphyrins are known as endogenous ligands for Translocator protein

MTT assay and fluorescence microscopy were utilized in C6 cells

Swelling study and rheological study were used to analyze the viscoelastic properties

Proven cellular uptake and cytotoxicity in vivo

Excellent stability and controlled release of NG system

TMZ&PTX [191]

TMZ@PTX@PEG-DMA

Intratumoral implantation was used instead modifications on NG

Clonogenic assay was conducted

Orthotopic U87MG human GBM tumor resection nude mice model was estabilished

Synergistic effect of PTX and TMZ on U87MG cells

Perisurgical drug delivery in the resection cavity

Cisplatin [192]

CPT@Cx43 mAb@BSAT1 mAb@NG

The preferential expression of membrane protein connexin 43 (Cx43) and brain-specific anion transporter (BSAT1) in the tumor was employed for targeted drug delivery

MTS assay was used to evaluate in vitro cytotoxicity on C6 cells

Intracranial inoculation of rat glioma 101/8 was constructed

Tumor volume was determined by MRI scanning

Higher passive penetration across endothelial barrier

Increased drug delivery efficacy and internalization in tumor site

Prolonged survival time for animal model

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