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Table 2 Different approaches for manufacturing of various nanomaterials with their respective types

From: Nanotechnology: from In Vivo Imaging System to Controlled Drug Delivery

Approach

Subtypes

Principle

Example of drug

Nanostructure/nanodevice

References

Nanoprecipitation-dependent techniques

Anti-solvent precipitation

Supersaturation in which dissolution of a lipophilic drug in organic solvent followed by in anti-solvent (water).

It leads to the nucleation of drug followed by precipitation of particles.

Itraconazole

Amorphous nanoparticles (<250 nm)

[149]

[150]

Curcumin

Nanoparticles

[151]

Flash nanoprecipitation

Dissolution of a hydrophobic drug and amphiphilic copolymers in a water miscible organic solvent. Then, the organic solvent is mixed with an anti-solvent (water). High supersaturation level is achieved that triggers nanoprecipitaion.

Curcumin

Nanoparticles (40 nm)

[152]

AIE (aggregation-induced emission) active dye of EDP

Fluorescent nanoparticles (20–60 nm)

[153]

Doxorubicin

Nanoparticles (<100 nm)

[154]

Sono precipitation

Crystallization by ultrasonic waves

Fenofibrate

Nanocrystals

[155]

Felodipine

Nanosuspension

[156].

Herceptin (HCT)-functionalized paclitaxel

Nanocrystals

[157]

Lovastatin

Rod shaped nanocrystals

[158]

High gravity controlled precipitation

High gravity conditions are maintained for precipitation by passing solution across rotating bed packing.

Hydroxyapatite (nHAP)

Nanoparticles (1.9–14.2 nm)

[159]

Milling-dependent techniques

Wet milling technique

Attrition is involved in which microsized particles are commuted by milling beads in a milling chamber to obtain nanosized particles (usually smaller than 400 nm).

Griseofulvin and Indomethacin

Nanoparticles (<100 nm)

[160]

Itraconazole adipic acid

Nanocrystals

[161]

Repaglinide

Nanocrystals

[162]

Salt-assisted milling

Milling along with salts like NaCl with steel balls to produce nanosized particles.

NaCl is incorporated in milling medium to prevent degradation and aggregation of nanoparticles [28].

Nanodiamond aggregates (50–1000 nm)

Nanodiamond colloids (5–10 nm)

[163]

Co-grinding

Grinding of APIs with specific additives to produce nanosized particles

[164].

Ibuprofen–glucosamine HCl

Co-ground particles

[165]

Piroxicam

Cryogenic co-ground solid dispersions

[166]

High-pressure homogenization

 

Milling of suspended drug particles under high pressure by using homogenizer.

Myricetin

Nanosuspension

[167]

α-chitin

Nanofibers (<100 nm)

[168]

Spraying-dependent techniques

Spray drying

Dispersion or liquids are transformed into solid powdered form upon spraying into drying medium at high temperature [169].

Cyclosporine A

Nanoparticles (317 to 681 nm)

[170]

Electrospraying

Strong electric field is applied to atomize a liquid into fine dispersed particles at normal pressure and ambient temperature and without use of surfactants.

Piroxicam

Nanospheres

[171]

Supercritical fluid technology

RESS (Rapid expansion in supercritical solution)

Drug is solubilized in a supercritical fluid and the solution is then expanded in a low-pressure area through a nozzle.

The drug becomes insoluble in low pressure gas and then supersaturation occurs and this leads to the production of micro and nanosized particles.

Olanzapine

Nanoparticles (150–350 nm)

[172]

RESS-SC (Rapid expansion of supercritical solution with solid co-solvent)

In this technique, supercritical fluid, i.e., CO2, is saturated with several solid co solvents [173].

Theophylline

Nanoparticles (mean size: 85 nm)

[173]

SAS (supercritical anti-solvent)

In this technique, precipitation of drug occurs upon its dissolution in an organic solvent, due to antisolvent effect.

Polyvinylpyrrolidone (PVP)–folic acid (FA)

Microspheres

[174]

BSA (bovine serum albumin)

Nanoparticles (60 nm ± 10 nm)

[174]

SAA (supercritical-assisted atomization)

The organic solution and supercritical carbon dioxide (SC-CO2) are mixed; they form an expanded liquid in a saturator.

It is then atomized under some specific conditions results in the formation of nanodroplets which produce NPs by drying [175].

Rifampicin

PLLA nanoparticles (123 to 148 nm)

[176]

Gentamycin sulfate

Microparticles (<2 μm)

[177]

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