From: Advanced application of nanotechnology in active constituents of Traditional Chinese Medicines
Nanocarriers | Materials | TCMs | Advantages | References |
---|---|---|---|---|
Liposomes | Lecithin-chitosan lipid polymer | Curcumin | High encapsulation; stable in the pH of 2–6; enhanced antioxidant | [267] |
phospholipid | Genistein | Higher bioavailability; enhanced liver homogenate lipid peroxidation property; histopathological alterations in liver and kidney | [412] | |
Hexadecyl palmitate; squalene; soybean phosphatidylcholine; | Silibinin | Slower silibinin release; enhanced therapeutic efficiency and a reduction of adverse responses | [269] | |
Lipid glycerol monooleate; polysorbate 80 | Brucea javanica oil | Stealth properties and colloidal stability; 90% encapsulation efficiency rate; enhanced anti-tumor efficiency; | [270] | |
Phosphatidylcholine; phosphatidylethanolamine; phosphatidylinositol; phosphatidic acid; glycolipids; neutral lipids; chondroitin sulfate | Anthocyanins | Enhanced stability and bioavailability; higher encapsulation efficiency; increased number of apoptotic cancer cells; reduced degradation and preserved antioxidant activity | ||
Soybean phospholipid; cholesterol | Tanshinone II A | Inhibit the proliferation of human HSCs; sustained release trend | [276] | |
mPEG2000-DSPE; Dipalmitoylphosphatidylcholine; lecithin; cholesterol | Glycyrrhizic acid; silybin | Increment of co-entrapment; suitable EE, stability, controlled release of drugs; lower IC50 on the HepG2 cancer cell line | [277] | |
Solid lipid nanoparticles (SLNs) | Glycerin monostearate; poloxamer; CPT-SS-PA conjugate | CPT | Great association efficiency; high stability in neutral medium and simulated gastrointestinal fluids; great cytotoxicity to various cancer cell line; enhanced oral bioavailability | [286] |
Nanostructured lipid carriers (NLCs) | Soy lecithin; glyceryl; tridecanoate; glyceryl tripalmitate; vitamin E acetate; Kolliphor HS15 | Resveratrol | Showing stability in artificial gastric and/or intestinal fluids; significant anticancer activity against Hep-G2, human HCT-116, lymphoblastic leukemia cells (1301), and human MCF-7 cell lines; significant apoptotic properties; potent in vitro antioxidant activity | [294] |
Compritol; labrafil 1944; lecithin; Tween-80 | ART | Small particle size; good stability; high entrapment efficiency; sustainably release; more cytotoxic than free ART; apoptosis of tumor cells | [295] | |
Octyl decyl acid triglycerate; Tween-80; lecithin; Poloxamer 188; monostearin | Curcumin | Superior anti-cancer activity in inhibiting proliferation; inducing apoptosis of human HepG2 cells; increased total expression of DR5 protein; upregulated cell membrane expression of DR5 | [296] | |
Solid lipid (Cap MCM C10); liquid lipid (Capmul PG8); Tween 80; PL-90G | Ganoderic acid | Compatible in hepatic nodules, hepatic, non-hepatic, antioxidant parameters, in a significant manner (p < 0.001); interferes with various cancer signaling protein | [297] | |
Microemulsion and nanoemulsion | R9 peptide; egg phosphatidylcholine; Mal-PEG-DSPE; PEG-DSPE; soya bean oil | Curcumin | Low cytotoxicity on HEC and low haemolytic activity; anti-inflammatory effect; increased accumulation of R9-CmLN in liver and lungs | [310] |
Ethosomes and transfersomes | Folate-modified TPGS; PEG1000; cholesterol | Docetaxel | Low particles sizes and polydispersity index; high encapsulation efficiency; higher permeability into 3D U-87 MG spheroid; selectivity of transfersomes to tumoral cells | [269] |
HSPC; DSPE-PEG2000; cholesterol | Eugenol and cinnamaldehyde | Improved formulation stability and percutaneous drug absorption; increase interstitial cells of Cajal; excellent deformability; improved efficacy against UC | [324] | |
Polymer micelles (PMs) | PEGylated PLGA polymer (Resomer® RGPd50105 and RGPd5055; | Digoxin | Across BeWo b30 cell monolayers easily; high encapsulation efficiency and sustained release; increased the permeability of digoxin | [418] |
Chondroitin sulfate; | Docetaxel | High permeability and cytotoxicity of Cys-DTX prodrug, targeting transportation of encapsulated redox-responsive Cys-DTX prodrug; improved permeability in tumor tissues, enhanced cytotoxicity and decreased side effects | [398] | |
Cystamine; Xanthan gum | Resveratrol | Good redox responsiveness; biocompatible; controlled in vitro drug release similar to the internal environment of tumor cells | [333] | |
PEG-40 hydrogenated castor oil | Curcuminoid | Physically stable for at least two months; uniform droplets size and low polydispersity | [419] | |
Polymeric vesicles | (Poly (ethylene glycol)-b-poly (propylene thioether) (PEG-b-PPS)) | Hydroxychloroquine (HCQ); tunicamycin (Tuni) | Simultaneously inducing endoplasmic reticulum (ER) stress and autophagic flux blockade; inhibiting tumor metastasis | [344] |
PEG-PLA/PEG-PBD hybrid vesicles | Paclitaxel | Thick hydrophobic membrane and an aqueous lumen to efficiently carry both hydrophobic and hydrophilic drugs; higher maximum tolerated dose; controlled drug release; two-fold higher cell death in tumors than free drug | [345] | |
Polymer hydrogels | Poly(N-isopropylacrylamide) and PEG | Artemisinin | Maintain the drug concentration at a therapeutic level for up to 10Â days | [351] |
Poloxamer and chitosan | Herbal formula | Sustained release and enhanced nasal absorption of the active compounds | [353] | |
Gold nanoparticles (Au NPs) | DO powder; AuNPs | Dendrobium officinale (DO) | Better anti-tumor efficiency compared with DO extraction alone without increasing toxicity in vivo and in vitro | [362] |
AuNPs | Licochalcone A | Increased solubility in aqueous solution; green method | ||
AuNPs | Pholiota adiposa | Significantly improved immune regulation and anti-tumor effect in comparison; no toxicity both in vivo and in vitro | [365] | |
AuNPs | Paeonia mountan | Fulfills the requirement of ideal nanodrug and it potentially inhibited the inflammation in in vitro murine microglial BV2; alleviates the neuroinflammation and improves the motor coordination in Parkinson induced mice | [366] | |
Mesoporous silica nanoparticles (MSNs) | Pluronic F127; CTAB; TWEEN20; MSNs | Resveratrol | Solubility, drug release, and transport enhancement of resveratrol; enhanced anti-inflammatory activity | [372] |
Lipid-coated MSN@p(NIPAM-co-MA) | EVO; BBR | Improved efficacy and biocompatibility of the drug pair; desirable drug profiles at the low pH and higher temperature of the tumor microenvironment; excellent synergistic therapy effects in vitro and in vivo; lower systemic toxicity | [374] | |
Hyaluronan (HA) or polyethyleneimine-FA (PEI-FA); MSNs | Curcumin | More precise targeting and higher accumulation in tumors; good biocompatibility and low toxicity; inhibited the tumor growth to a greater degree | [375] | |
FA–conjugated mesoporous silica nanoparticles (FA-MSNs) | Rhodojaponin III | Prolonged RJ-III release in vitro; reduced the cytotoxicity of RJ-III (P < 0.01); good targeting effect; improved the LD50 value of RJ-III in mice | [376] | |
Organic/Inorganic Nanohybrids | Indocyanine green (ICG); perfluoropentane (PFP); MSNs; PEG | Paclitaxel | Effective intracellular ICG deliver; NIR-responsive hyperthermia; permitting photothermal therapy and photoacoustic imaging; potent and synergistic chemo-photothermal therapy | [382] |
PEG-b-P(CPTM-co-MPS) and PEG-b-P(CPTHM-co-MPS) | CPT | Codelivery both hydrophobic and hydrophilic drugs; site-specific synchronized corelease enhanced combination chemotherapeutic efficacy and reduced systemic toxicity | [384] | |
 | N-(2-hydroxypropyl methyl) acrylamide (HPMA) copolymer-gadolinium-paclitaxel-Cyanine5.5 (pHPMA-Gd-PTX-Cy5.5) | Paclitaxel | Enhanced imaging capacity of the theranostic nanomedicine; residence time significantly prolonged; increased accumulation at the tumor site; inhibited proliferation and induced apoptosis of the 4T1 murine breast cancer cells | [420] |
 | Monomethoxy-poly(ethylene glycol)-b-poly(lactide) (mPEG-PLA) | Docetaxel | Clear spherical shape; sustained release of the drug; time-dependent anticancer effect in the squamous cancer cells; significantly higher cancer cell apoptosis in HSC-3 cancer cells; controlled the tumor progression in HSC-3 cancer cells | [400] |
 | Polyethylene glycol-BA (PEG-BA) | BA | Increased NFκB/p65 protein expression; comparable antioxidant potential with ascorbic acid; improved reduction of hydroperoxide levels | [399] |
Nanocarriers based on active ingredients from TCMs | Baicalin and flavonoid glycosides | Baicalin and flavonoid glycosides | Significantly enhanced bacteriostatic activity; stronger affinity to bacteria; good biocompatibility; excellent antibacterial performance | [409] |
BBR and cinnamic acid | BBR and Cinnamic acid | better inhibitory effect on multidrug-resistant S. aureus (MRSA) and stronger ability for biofilm removal; nonhemolytic with little toxicity in vitro and in vivo | [412] | |
Lipophilic alkyl BBR derivatives (BDs) and rhamnolipids (RHL) | BDs and RHL | Enhanced hydrophilicity, successfully penetrated through mucus layer without interacting with mucins; substantial ability to eradicate H. pylori biofilms; inhibited the adherence of H. pylori on both biotic and abiotic surfaces | [413] | |
Ursolic acid | Ursolic acid | Near-spherical shape; higher antiproliferative activity; significantly caused apoptosis; decreased the expression of COX-2/VEGFR2/VEGFA; increased the immunostimulatory activity of TNF-α, IL-6, and IFN-β; inhibiting tumor growth and having the ability of liver protection in vivo | [408] | |
Poria cocos; Liquidambar formosana | Poria cocos; Liquidambar formosana; PTX | Improved therapeutic effect on tumors through synergistic action; reducing chemotherapeutic cardiotoxicity and prolonging survival; superior anti-inflammatory efficacy | [409] | |
Ursolic acid and PTX | Ursolic acid and PTX | Facile structure regulation and drug loading; synergistic therapeutic efficacy; reducing the risk of liver damage; benefiting and eliminating the trouble of the toxic side effects | [414] |