From: Extracellular vesicles: a rising star for therapeutics and drug delivery
EVs loading | Source | Loading methods | Size (nm) | Zeta potential(mV) | Cargos | Loading efficiency | Functions | Refs. |
---|---|---|---|---|---|---|---|---|
Pre-loading | ADMSCs | Incubation | sEV-CUR: 74.05 ± 2.52 |  N/A | Curcumin | 82.26 ± 5.25% | Excellent anti-oxidative and anti-apoptotic capacity; Favorable bioavailability; Controlled release | [110] |
 | HEK293T | Incubation | EVs (ICG/PTX): 149.9 ± 5.2 | -30.2 | ICG/PTX | ICG: 60.7%; PTX: 51.9% | Simultaneous therapy and high accumulation at the tumor site; High encapsulation efficiency and cellular uptake; Photo-stability and storage stability | [111] |
 | HL-60; dHL60; MCF-7; THP-1 | Infection | HL-60: 170.5 ± 49.4; dHL-60: 246.8 ± 19.5 |  N/A | Penicillin/ PTX /MCP-1/MiR-16/Cas-9-GFP/Cas9 | N/A | High encapsulation efficiency and production efficiency; Low immunogenicity | [112] |
 | MSCs | Infection and incubation | 60–150 |  N/A | CTX/TRA-IL | 15.43 ± 0.44% | Synergistic effects and few side effects | [113] |
 | ADSCs | Infection | 30–150 |  N/A | NT-3 siRNA | N/A | Stable and functional delivery | [114] |
 | HUVECs | USMB | N/A | N/A | CTG/BSA-FITC | N/A | High encapsulation efficiency and improved EVs production | [115] |
Post-loading | RAW 264.7 | Incubation | 100–200 |  N/A | HA/CV/D-OX | N/A | Polarization to M1 macrophages; High cellular uptake; Excellent antitumor effect | [117] |
 | THP-1 | Incubation | A15-Exo: 94.1 ± 104.4 | A15-Exo: − 9.68 ± 0.29 | DOX | NA | Targeting ability; high yield; efficient release | [118] |
 | A549 | Incubation | DOX/LND-16k: 93.2 ± 24.2; DOX/LND-120k: 70 ± 11.1 | DOX/LND-16k: -15.2; DOX/LND-120k: -15.9 | DOX/LN-D | DOX/LND-16k: 4.16 ± 1.9%; DOX/LND-120k: 2.77 ± 0.35% | Excellent anticancer effect (DNA damage, ATP inhibition, and ROS generation) | [119] |
 | Macrophage | Sonication | 115.0 ± 8.3 |  N/A | TPP1 | N/A | High loading capacity; Sustained release; Bio-inspired; Non-viral and favorable stability | [243] |
DOX: 162.2 ± 1.6; PTX: 129.4 ± 2.3 |  N/A | DOX/PT-X | N/A | Superior intracellular accumulation and drug accumulation in cancer cells; Low immunogenicity and favorable stability | [120] | |||
 | hMSCs | Electroporation | ~ 210 | ~ -10 | GPX4 siRNA | 16.6% | Magnetic targeting; BBB penetration ability; Synergistic ferroptosis therapy; Good biocompatibility and safety | [123] |
 | 4T1 | Extrusion | MSNs: 125 ± 15; E-MSNs: 150 ± 11 | MSNs: 20.5 ± 1.2; ID@MS-Ns: -5.8 ± 1.5; ID@E-MSNs: -28.9 ± 3 | ICG/DOX | N/A | High cellular uptake and long-term retention; Synergistic chemo-photothermal therapy; High purity; Favorable biocompatibility | [125] |
 | MSCs | Extrusion | 135.9–194.9 | -7.23 | Curcumin | 75.53% | Relieves neuroinflammation | [126] |
 | 4T1 | Extrusion | 173 | N/A | DOX | 7.4% | Prominent biocompatibility; Synergistic photothermal properties; Controlled release drug; Good stability | [127] |
 | U87; U251 | Saponin | U87-sEVs: 76.71 ± 21.7; U251-sEVs: 79.11 ± 28.77 | ~ -12.5 | DOX | N/A | Excellent anti-oxidative and anti-apoptosis ability; Favorable bioavailability; Controlled release; Outstanding stability | [129] |
 | U251-GMs; SF7761- GMs | Microfluidics | U251GMs: 150 SF7761 GMs: 100 |  N/A | DOX | U251GMs: 31.98%; SF7761 GMs: 19.7% | Homing effect; Simple; Efficient setup; Adjustable condition | [132] |
 | Human plasma | Acoustofluidics | N/A | N/A | DOX | ~ 30% | High loading efficiency; One-step process; Rapid encapsulation | [133] |