| Literature DB >> 31216688 |
Lili Wang1, Xiaowei Liu2,3.
Abstract
Sustained release technology is a class of technology characterized by slowly-releasing specific active substances into a target medium to keep a certain concentration in the system within valid time. As a new of type technology, it has been extensively applied to medicine, chemical engineering, agriculture, environmental protection, etc. The principles and classification of sustained release technologies, as well as typical preparation methods of sustained release agents, were summarized in this paper; by introducing applied research progress of sustained release technologies into environmental fields like rainwater purification, sewage/drinking water treatment, and soil and atmosphere remediation, application features of these sustained release technologies were evaluated, and their application prospect in environmental remediation, especially in water treatment, was predicted.Entities:
Keywords: classification; environmental remediation; preparation methods; sustained release technology
Mesh:
Substances:
Year: 2019 PMID: 31216688 PMCID: PMC6617011 DOI: 10.3390/ijerph16122153
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 3.390
Formulation methods and principles of typical sustained release agents.
| Morphology of Sustained Release Agent | Preparation Method | Preparation Principles and Features |
|---|---|---|
|
| Complex coacervation | Two macromolecular molecules with opposite charges are taken as composite capsule materials which cross-link with each other under certain conditions and experience coacervation with capsule core to form capsules [ |
| Simple coacervation | Coagulant is added in macromolecular capsule material solution to reduce macromolecular solubility for coacervation into capsules [ | |
| Solvent/non-solvent method | According to the solubility principle, target substance is firstly dissolved in a solvent, followed by necessary operations, and then nonsolvent chemicals are added so that target substance is precipitated out in the form of crystallization or wrapping on other material surfaces [ | |
| Drying in liquid technique | The volatile solvent in the disperse phase is removed from the emulsion to prepare microcapsules (microspheres) [ | |
| Spray drying method | After thinner is atomized in a drying room, moisture will be rapidly vaporized when thinner contacts hot air so as to obtain the dry product. This method can directly dry solution and emulsion into powdery or particulate products, thus saving evaporation, crushing and other procedures. | |
| Spray congealing | After being dissolved with a proper solvent, the drug is blended with the molten carrier, and the product can be obtained after cooling and congealing. | |
| Self-assembly method | The principle of molecular self-assembly is to use molecular recognition between a molecule pair or fragment pair to form a class of molecular polymers with a specific structure, stability, and specific properties through non-covalent interaction [ | |
| Fluidized bed coating | Capsule core is suspended in the coating room through vertical strong airflow. Capsule solution is sprayed onto the surface of capsule core through a nozzle so that hot airflow resulting in the suspension of capsule core volatilizes the solvent until it becomes dry, and then thin capsule film is formed on the surface to obtain microspheres. | |
| Multiorifice-centrifugal process | Drug obtain centrifugal force through a high-speed revolution cylinder. The drug solution passes through the capsule material at a high speed to form a liquid film which is then solidified through different methods to obtain microspheres [ | |
| Supercritical fluids | The drug solution is dispersed in supercritical fluid through the nozzle of a supercritical fluid device, the organic solvent is dissolved in a supercritical fluid and then extracted, and the remaining drug is formed into microspheres [ | |
| Spinning disk atomization | The material enters a disk spinning at a high speed through the material supply tube. Under high-speed shear action, it leaves the edge of the disk and solidified after being cooled at the bottom, thus forming microspheres [ | |
| Interface polycondensation | Capsule film is generated due to monomer polycondensation reaction on the interface of the disperse phase (aqueous phase) and continuous phase (organic phase), thus forming microspheres [ | |
| Chemical radiation | γ-ray energy generated by 60Co is used for cross-linking and congealing of polymer (gelatin or polyvinyl alcohol) so as to form microspheres [ | |
|
| Adsorption method | Active substances are adsorbed through many pores or high specific surface area to reach the sustained release effect [ |
|
| Drying or wetting method for particle/tablet preparation | Skeleton material, drug, and other ingredients are blended to directly prepare particles/tablets, and in some cases, the adhesive or wetting agent is used to help the particle/tablet preparation [ |
|
| Solid dispersion method | The drug is incorporated into a solid carrier under a highly dispersed state through certain methods (melting method, solvent method, and mechanical dispersion method) [ |
|
| Emulsion polymerization | The monomer is firstly dispersed in aqueous capsule emulsion droplets containing an emulsifier, it is polymerized into nanoparticles using methods such as high-energy radiation and then turned into the solid state after phase separation, and then solid nanoparticles are prepared [ |
| Natural polymer condensation method | Natural macromolecular (like protein and polysaccharides) solution containing active components is added into the oil phase and then water/oil emulsion is formed through mechanical agitation or ultrasonic dispersion. Macromolecules are condensed through chemical crosslinking, thermotropy or dehydration by salting-out under proper conditions, thus forming nanoparticles [ |