| Literature DB >> 35189225 |
Bing Li1, Yuxiong Huang2, Dengting Guo3, Yuzhi Liu2, Ziyi Liu2, Jing-Cheng Han4, Jian Zhao5, Xiaoshan Zhu6, Yuefei Huang1, Zhenyu Wang7, Baoshan Xing8.
Abstract
Since the COVID-19 outbreak in early 2020, face mask (FM) has been recognized as an effective measure to reduce the infection, increasing its consumption across the world. However, the large amount of at-home FM usage changed traditional medical waste management practices, lack of improper management. Currently, few studies estimate FM consumption at a global scale, not to say a comprehensive investigation on the environmental risks of FM from a life cycle perspective. Therefore, global FM consumption and its associated environmental risks are clarified in the present study. Our result shows that 449.5 billion FMs were consumed from January 2020 to March 2021, with an average of 59.4 FMs per person worldwide. This review also provides a basis to understand the environmental risk of randomly disposed of FM and highlights the urgent requirement for the attention of FMs waste management to prevent pollution in the near future.Entities:
Keywords: COVID-19; Face mask; Microplastics; Plastic pollution; Toxic chemicals
Mesh:
Substances:
Year: 2022 PMID: 35189225 PMCID: PMC8855619 DOI: 10.1016/j.scitotenv.2022.153880
Source DB: PubMed Journal: Sci Total Environ ISSN: 0048-9697 Impact factor: 10.753
Fig. 2Used FMs found at Hongkong (a) coastal beach (b) and local environment (c). Note: 5 used FMs found at a very small beach (b) in one afternoon; 22 used FMs were randomly found at a very small local environment (c, including street, bus station, play and rest area, pet garden, et al) in one week.
Fig. 1The life cycle of disposable FMs in the environment.
Health and ecological effects of the main compounds in inks and dyes (Schmid and Speit, 2007; Jammalamadaka and Raissi, 2010; Neghab et al., 2015; Crowell et al., 2015).
| Compounds | Structure | Organism | Remarks |
|---|---|---|---|
| BTEX | Human | Evident dysfunction in kidney and liver. | |
| Ethyl acetate | Rats, human | Decreased respiratory rate and tidal volume; Impair neurological function; Lower blood concentrations. | |
| Isopropanol | Human | Nausea, vomiting, abdominal pain, gastritis, headache, dizziness, confusion, stupor, and coma. | |
| Formaldehyde | Human | FA-induced cytotoxicity (measured as reduction of the nuclear division index) possibly prevented division of damaged cells. | |
| Acetaldehyde | Human | The deficient expression of aldehyde dehydrogenase (ALDH) I will cause elevated concentrations of acetaldehyde in blood, exhibiting characteristic clinical symptoms, such as peripheral vasodilation, flushing, changes in heart rate, difficulties in breathing, and muscle weakness. | |
| Acetic Acid | Budding Yeast | A mechanism of acetic acid toxicity in yeast is related to the induction of growth signaling pathways and oxidative stress. These mechanisms are relevant to aging in all eukaryotes. | |
| Propanone | Sprague–Dawley Rats | Markedly decreased locomotor activity in animals on acetone-paired days compared to air-paired days. | |
| Acetophenone | Rabbit | Standard Draize test; Severe reaction severity. | |
| Diphenyl ether | Rabbit | Standard Draize test; Mild reaction severity. | |
| 2,5-Cyclohexadiene-1,4-dione | Mouse | Tumorigenic in lungs, thorax, or respiration, skin, and appendages. | |
| Butylated Hydroxytoluene | Mouse | Tumorigenic in lungs, thorax, or respiration, skin and appendages. | |
| Isopropyl myristate | Guinea Pig | Standard Draize test; Administration onto the skin; Moderate reaction severity. | |
| Isopropyl palmitate | Rabbit | Standard Draize test; Administration onto the skin; Moderate reaction severity. | |
| Pyrene | Mouse | Tumorigenic in skin and appendages. | |
| Tributyl acetylcitrate | Mouse | Pigmented or nucleated red blood cells; Blood changes in erythrocyte (RBC) count; Weight loss or decreased weight gain. | |
| Ethanol, 2-phenoxy- | Rat | Changes in bladder weight; Weight loss or decreased weight gain; Death. | |
| Octane, 1,1′-oxybis- | Mouse | LD50: 1183 mg/kg. | |
| Butyraldehyde | Rat | Other changes in lungs, thorax, or respiration; transaminases; Death. | |
| Acetylacetone | Rat | Changes in thymus weight; Weight loss or decreased weight gain. | |
| Rat | Lethal dose, 50% death; Oral; 25,800 mg/kg dose; Coma; Cyanosis; Gastrointestinal hypermotility or diarrhea. |
Potential risks of additives used in plastic production.
| Compound | Structure | Organism | Remark | Ref. |
|---|---|---|---|---|
| Plasticizers | ||||
| DEHP | Catfish | Damage liver; ROS; lipid peroxidation, immunosuppression. | ( | |
| DEP | Shorten the lifespan and decreased reproduction rate. | ( | ||
| DIDP | Zebrafish ( | Oxidative stress reactions; Disruption in circadian rhythm. | ( | |
| DINP | Zebrafish ( | Effects on oocytes growth maturation, gonadal development and reproduction; Impair endocannabinoid system. | ( | |
| Antioxidants | ||||
| BHT | Zebrafish ( | Cardiotoxicity and developmental toxicity. | ( | |
| BHA | Rat liver | ROS production. | ( | |
| Stabilizers | ||||
| BPA | Zebrafish ( | Acute metabolic effects in larvae; Effects on hatchability and heart rates; Craniofacial deformity; Elongation of head length. | ( | |
| NP | Mullets | Adverse impact on cell membrane and cellular metabolism. | ( | |
DEHP: Di-(2-ethylhexyl) phthalate; DEP: diethyl phthalate; DIDP: Diisodecyl phthalate; DINP: Diisononyl phthalate;
Halogen: Bromine and chlorine; BHT: 2,6-di-tert-butyl-4-methylphenol; BHA; Butyl hydroxyanisole; BPA: Bisphenol A.
Ecological risks of heavy metals engaged within FMs.
| Heavy metal | Organism | Remark | Ref. |
|---|---|---|---|
| Cr | Mouse | No mutagenic effect of CrCl3; Severe acute toxicity of K2Cr2O7 (as the mutagen). | ( |
| Pb | Mouse | Significant reduction in serum testosterone, serum and testicular E2; Testicular testosterone increase. | ( |
| Ti | Toxic; Nano-TiO2 could dissociate adsorbed As (V). | ( | |
| Zn | A significant time and dose effect relationship between the heavy metal Zn2+ treatment and DNA damage in hepatopancreas of loach. | ( | |
| Cu | Different degrees of liver tissue damage. | ( | |
| Ag+, Ag2+, Ag3+ | Zebrafish | Increased mortality, decreased hatching rate, and delayed hatching with a concentration-dependent manner. | ( |
| Al | Human | An association between chronic Al exposure and impaired cognitive function in majority of domains including memory, processing speed, and working memory. | ( |
| Fe | Medaka Fish | Different antioxidant balance by induced intracellular ROS in hatchlings with three iron species. | ( |
The adsorption capacity of heavy metals and organic pollutants by microplastics.
| Pollutants | Adsorption particles | Adsorption capacity (μg/g) | Remarks | Ref. | |
|---|---|---|---|---|---|
| Heavy metals | Pb | PE MPs; PP | / | Cr and Pb: Stronger adsorption capacity to PE; PP: Pb > Cd > Cu. | ( |
| Cd | LDPE microbeads; PE MPs; PP | 10.1; <0.8 | |||
| Cr | LDPE microbeads; PE beads | 1.7; 1360 | |||
| Cu | PE MPs; PP | 31.2; 42.6; <0.8 | |||
| Zn, Cs | PE MPs | <0.8 | |||
| Organic contaminants | PAHs | LDPE; PE, PVC | 69.8–159.5 | Phenanthrene: Strongest adsorption capacity to LDPE; Nonylphenols: CIP: Strongest adsorption capacity to PP; CIP: Strongest adsorption capacity to PE; levofloxacin and DIFE: Strongest adsorption capacity to PVC. | ( |
| PCBs, DDE, and NP | PP | 1.6 × 10−4–16 | |||
| Pharmaceuticals | PE, PVC | 46.1–1740 | |||
| Pesticides | PE | 2.9–273.2 | |||
| Antibiotics | PE | 61–963 | |||
PAHs: Polycyclic aromatic hydrocarbons; HDPE: High-pressure polyethylene.
PCBs: Polychlorinated biphenyls; DDE: 1,1-Bis (p-chlorophenyl) - 2,2-dichloroethylene; Pharmaceuticals: including sulfamethoxazole(SMX), propranolol (PRP), sertraline (SER), amoxicillin (AMX), ciprofloxacin (CIP); trimethoprim(TMP) and levofloxacin; Pesticides: including carbendazim(CAR), dipterex (DIP), diflubenzuron (DIF), malathion (MAL) and difenoconazole (DIFE).