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1.
Environ Res ; 223: 115408, 2023 04 15.
Article in English | MEDLINE | ID: mdl-36740151

ABSTRACT

Increased environmental pollution is a critical issue that must be addressed. Photocatalytic, adsorption, and membrane filtration methods are suitable in environmental governance because of their high selectivity, low cost, environment-friendly nature, and excellent treatment efficiency. Graphitic carbon nitride (g-C3N4) quantum dots (QDs) have been considered as photocatalysts, adsorbents, and membrane materials for wastewater treatments, owing to their stability, adsorption capacity, photochemical properties, and low toxicity and cost. This review summarizes g-C3N4 QD synthesis techniques, operating parameters affecting the removal performance in the treatment process, modification effects with other semiconductors, and benefits and drawbacks of g-C3N4 QD-based materials. Furthermore, this review discusses the practical applications of g-C3N4 QDs as adsorbents, photocatalysts, and membrane materials for organic and inorganic contaminant treatments and their value-added product formation potential. Modified g-C3N4 QD-based material adsorbents, photocatalysts, and membranes present potentially applicable effects, such as removal of most waterborne contaminants. Excellent results were obtained for the reduction of methyl orange, bisphenol A, tetracycline, ciprofloxacin, phenol, rhodamine B, E. coli, and Hg. Overall, this paper provides comprehensive background on g-C3N4 QD-based materials and their diverse applications in wastewater treatment, and it presents a foundation for the enhancement of similar unique materials in the future.


Subject(s)
Quantum Dots , Wastewater , Quantum Dots/chemistry , Conservation of Natural Resources , Escherichia coli , Environmental Policy , Catalysis
2.
J Eur Acad Dermatol Venereol ; 34(6): 1348-1354, 2020 Jun.
Article in English | MEDLINE | ID: mdl-31954062

ABSTRACT

BACKGROUND: Erosive pustular dermatosis of the scalp (EPDS) is characterized by crusted erosions or superficial ulcerations that lead to scarring alopecia. OBJECTIVES AND METHODS: We performed a multicentre retrospective clinical study including 56 patients (29 females and 27 males, mean age 62.7) with a confirmed EPDS in order to describe epidemiology, clinical findings and therapeutic choices of this disease. RESULTS: Mechanical/chemical trauma was reported in 28.6%, a previous infection in 10.7%, a previous cryotherapy in 5.4% androgenetic alopecia in 48.2% and severe actinic damage in 25%. Trichoscopy showed absence of follicular ostia, tufted and broken hair, crusts, serous exudate, dilated vessels, pustules and hyperkeratosis. Histopathology revealed three different features, depending on the disease duration. The most prescribed therapy was topical steroids (62.5%), followed by the combination of topical steroids and topical tacrolimus (8.9%), systemic steroids (7.1%) and topical tacrolimus (5.4%). A reduction of inflammatory signs was observed in 28 patients (50%) treated with topical steroids and in all three patients treated with topical tacrolimus. CONCLUSION: The relatively high number of patients collected allowed us to identify a better diagnostic approach, using trichoscopy and a more effective therapeutic strategy, with high-potency steroids or tacrolimus, which should be considered as first-line treatment.


Subject(s)
Scalp Dermatoses , Scalp , Alopecia/drug therapy , Alopecia/etiology , Female , Humans , Male , Middle Aged , Retrospective Studies , Scalp Dermatoses/diagnosis , Scalp Dermatoses/drug therapy , Tacrolimus/therapeutic use
3.
J Biol Regul Homeost Agents ; 33(3): 817-819, 2019.
Article in English | MEDLINE | ID: mdl-31184104

ABSTRACT

Pattern hair loss (i.e., androgenetic alopecia) is a common condition afflicting approximately fifty percent of men and women by the age of fifty. Currently, topical minoxidil is the only US FDA approved drug for the treatment of pattern hair loss in men and women.


Subject(s)
Alopecia/drug therapy , Minoxidil/pharmacology , Sulfotransferases/metabolism , Female , Humans , Male
4.
J Biol Regul Homeost Agents ; 32(4): 937-940, 2018.
Article in English | MEDLINE | ID: mdl-30043580

ABSTRACT

Minoxidil is the only US FDA-approved topical drug for the treatment of female and male pattern hair loss. Previously, it was demonstrated that topical minoxidil is metabolized to its active metabolite, minoxidil sulfate, by sulfotransferase enzymes located in the outer root sheath of hair follicles. The expression of sulfotransferase in the scalp varies greatly between individuals, and this difference in expression explains the varied response to minoxidil treatment. Previously, we have demonstrated the clinical utility of detecting sulfotransferase in plucked hair follicles to predict minoxidil response in pattern hair loss patients. Typically, exogenous exposure to substrates affects the expression of the enzymatic system responsible for their metabolism. For example, Phase I metabolizing enzymes, such as the cytochrome P450 family of enzymes, are known to be up-regulated in the presence of xenobiotic substrates. However, it is not known if Phase II metabolizing enzymes, such as the sulfotransferase family of enzymes, are similarly affected by the presence of substrates. In this study, we recruited 120 subjects and analyzed their sulfotransferase enzymatic activity before and after treatment with topical minoxidil. Adjusting the results for biologic (within subject) variability, we discovered that the sulfotransferase enzymatic system expression is stable over the course of minoxidil treatment. To the best of our knowledge, this is the first study to demonstrate the stability of sulfotransferase, a Phase II metabolizing enzyme, over the course of minoxidil treatment.


Subject(s)
Hair Follicle/drug effects , Hair Follicle/enzymology , Minoxidil/metabolism , Minoxidil/therapeutic use , Sulfotransferases/metabolism , Administration, Topical , Adult , Alopecia/drug therapy , Female , Humans , Male , Middle Aged
5.
Dermatol Ther ; 31(6): e12741, 2018 11.
Article in English | MEDLINE | ID: mdl-30226287

ABSTRACT

Topical minoxidil is the only US FDA approved OTC drug for the treatment of androgenetic alopecia (AGA). Minoxidil is a pro-drug converted into its active form, minoxidil sulfate, by the sulfotransferase enzymes in the outer root sheath of hair follicles. Previously, we demonstrated that sulfotransferase activity in hair follicles predicts response to topical minoxidil in the treatment of AGA. In the human liver, sulfotransferase activity is significantly inhibited by salicylic acid. Low-dose OTC aspirin (75-81 mg), a derivative of salicylic acid, is used by millions of people daily for the prevention of coronary heart disease and cancer. It is not known whether oral aspirin inhibits sulfotransferase activity in hair follicles, potentially affecting minoxidil response in AGA patients. In the present study, we determined the follicular sulfotransferase enzymatic activity following 14 days of oral aspirin administration. In our cohort of 24 subjects, 50% were initially predicted to be responders to minoxidil. However, following 14 days of aspirin administration, only 27% of the subjects were predicted to respond to topical minoxidil. To the best of our knowledge, this is the first study to report the effect of low-dose daily aspirin use on the efficacy of topical minoxidil.


Subject(s)
Alopecia/drug therapy , Aspirin/administration & dosage , Enzyme Inhibitors/administration & dosage , Hair Follicle/drug effects , Minoxidil/administration & dosage , Prodrugs/administration & dosage , Sulfotransferases/antagonists & inhibitors , Administration, Cutaneous , Adult , Alopecia/diagnosis , Alopecia/physiopathology , Aspirin/adverse effects , Drug Interactions , Enzyme Inhibitors/adverse effects , Hair Follicle/enzymology , Hair Follicle/growth & development , Humans , Male , Minoxidil/analogs & derivatives , Minoxidil/metabolism , Prodrugs/metabolism , Risk Assessment , Sulfotransferases/metabolism , Treatment Outcome , Young Adult
6.
J Biol Regul Homeost Agents ; 31(1): 237-238, 2017.
Article in English | MEDLINE | ID: mdl-28337898

ABSTRACT

Biological pigments or biochromes are ubiquitous in animals, plants, and simpler organisms such as fungi and bacteria. They serve a wide spectrum of functions from photosynthesis, camouflage, mimicry, photo protection from the environment to attracting mates. The human female nipple areola complex (NAC) is a highly-pigmented area. Currently, the prevailing theory as to the evolution of the pigmented human NAC is based on infant recognition of breast feeding latching zone; however, due to the protruding shape of the nipple and surrounding breast, the authors of this letter believe that the evolutionary advantage of the pigmented NAC has a direct physiological function, namely the initiation of involution at the end of the infant lactation period.


Subject(s)
Mammary Glands, Human/physiology , Melanins/biosynthesis , Nipples/physiology , Pigmentation/physiology , Adaptation, Physiological , Adult , Breast Feeding , Female , Humans , Infant , Mammary Glands, Human/anatomy & histology , Mammary Glands, Human/radiation effects , Nipples/anatomy & histology , Nipples/radiation effects , Ultraviolet Rays
7.
J Biol Regul Homeost Agents ; 31(3): 679-682, 2017.
Article in English | MEDLINE | ID: mdl-28956417

ABSTRACT

Herpes simplex encephalitis (HSE) is associated with significant mortality and morbidity. As a consequence of HSE, up to 75% of infected individuals die or experience irreversible neurological damage. While the pathogenesis of the disease is unknown, it is traditionally hypothesized that the viral infection occurs by neuronal transmission directly from peripheral sites. Non-neuronal modes of infection have generally been overlooked as the brain is protected by the blood-brain-barrier (BBB). The BBB poses an effective barrier to pathogens as well as to drugs such as chemotherapies. In the pursuit to deliver chemotherapeutic agents to the brain, several studies demonstrated that phosphodiesterase type 5 (PDE5) inhibitors, such as sildenafil, may increase the permeability of the BBB enabling successful delivery of chemotherapeutic agents to the brain. In this communication, we report a case of HSE infection in a 62-year-old man, which we suspect was facilitated by the use of sildenafil during a primary genital herpes simple virus (HSV) infection. Due to large number of patients treated with PDE5 inhibitors for erectile dysfunction and the high incidence of genital HSV infection in the general population, a larger study should examine the potential risk of developing HSE in patients treated with PDE5 inhibitors.


Subject(s)
Encephalitis, Herpes Simplex/chemically induced , Herpes Genitalis/drug therapy , Sildenafil Citrate/adverse effects , Blood-Brain Barrier/physiopathology , Encephalitis, Herpes Simplex/physiopathology , Encephalitis, Herpes Simplex/virology , Herpes Genitalis/physiopathology , Herpes Genitalis/virology , Humans , Male , Middle Aged , Permeability , Sildenafil Citrate/administration & dosage
8.
J Biol Regul Homeost Agents ; 31(4): 1049-1053, 2017.
Article in English | MEDLINE | ID: mdl-29254313

ABSTRACT

Topical minoxidil is the only topical drug approved by the US Food and Drug Administration (FDA) for the treatment of androgenetic alopecia. However, the exact mechanism by which minoxidil stimulates anagen phase and promotes hair growth is not fully understood. In the late telegen phase of the hair follicle growth cycle, stem cells located in the bulge region differentiate and re-enter anagen phase, a period of growth lasting 2-6 years. In androgenetic alopecia, the anagen phase is shortened and a progressive miniaturization of hair follicles occurs, eventually leading to hair loss. Several studies have demonstrated that minoxidil increases the amount of intracellular Ca2+, which has been shown to up-regulate the enzyme adenosine triphosphate (ATP) synthase. A recent study demonstrated that ATP synthase, independent of its role in ATP synthesis, promotes stem cell differentiation. As such, we propose that minoxidil induced Ca2+ influx can increase stem cell differentiation and may be a key factor in the mechanism by which minoxidil facilitates hair growth. Based on our theory, we provide a roadmap for the development of a new class of drugs for the treatment of androgenetic alopecia.


Subject(s)
Alopecia/drug therapy , Hair Follicle/drug effects , Minoxidil/therapeutic use , Mitochondria/drug effects , Mitochondrial Proton-Translocating ATPases/genetics , Stem Cells/drug effects , Vasodilator Agents/therapeutic use , Adult , Alopecia/enzymology , Alopecia/genetics , Alopecia/pathology , Calcium/metabolism , Cell Differentiation/drug effects , Gene Expression , Hair Follicle/enzymology , Hair Follicle/pathology , Humans , Ion Transport/drug effects , Male , Middle Aged , Mitochondria/enzymology , Mitochondrial Proton-Translocating ATPases/metabolism , Stem Cells/enzymology , Stem Cells/pathology , Up-Regulation
9.
J Biol Regul Homeost Agents ; 31(4): 1013-1016, 2017.
Article in English | MEDLINE | ID: mdl-29254307

ABSTRACT

In recent years, dermatologists have observed an increase in the incidence of male androgenetic alopecia (AGA). In a survey of 41 dermatologists, 88% reported an increase in incidence of AGA in men younger than 30 years. This phenomenon has no apparent explanation. However, due to the strong genetic inheritance component of AGA, a social or environmental factor which favours the inheritance of genes that increase the risk of developing AGA is suspected. To date, the strongest predictor of AGA in men has been the length of the CAG repeat located in the androgen receptor gene (AR gene) on the X chromosome. The same genetic variant in women is associated with ovulation at a later age, higher antral follicle count, and lower risk for premature ovarian failure. This led us to theorize that, due to social pressure to conceive later in life, women carriers of the short CAG repeat in the AR gene would have a selective advantage to conceive later in life and would thus favour male offspring exhibiting AGA.


Subject(s)
Alopecia/genetics , Genetic Predisposition to Disease , Maternal Inheritance , Receptors, Androgen/genetics , Adult , Age Factors , Alopecia/diagnosis , Chromosomes, Human, X/chemistry , Chromosomes, Human, X/metabolism , Female , Fertilization/genetics , Gene Expression , Humans , Male , Ovarian Follicle/cytology , Ovarian Follicle/physiology , Ovulation/genetics , Receptors, Androgen/chemistry , Selection, Genetic , Socioeconomic Factors , Trinucleotide Repeats
10.
J Biol Regul Homeost Agents ; 30(4): 1153-1155, 2016.
Article in English | MEDLINE | ID: mdl-28078868

ABSTRACT

Topical minoxidil is the only US FDA approved drug for the treatment of female pattern hair loss (FPHL). 5% minoxidil foam is only effective at re-growing hair in a minority of women (approximately 40%). Thus, the majority of FPHL patients remain untreated. Previously, we demonstrated that nonresponders to 5% minoxidil have low metabolism of minoxidil in hair follicles. As such, we hypothesized that increasing the dosage of topical minoxidil to low metabolizers would increase the number of responders without increasing the incidence of adverse events. In this study, we recruited FPHL subjects that were identified as non-responders to 5% topical minoxidil utilizing the previously validated assay for minoxidil response. Subjects were treated for 12 weeks with a novel 15% topical minoxidil solution. At 12 weeks, 60% of subjects achieved a clinically significant response based on target area hair counts (>13.7% from baseline), as well as significant improvement in global photographic assessment. None of the subjects experienced significant hemodynamic changes or any other adverse events. To the best of our knowledge, this is the first study to demonstrate the potentially beneficial effect of a higher dosage of minoxidil in FPHL subjects who fail to respond to 5% minoxidil.


Subject(s)
Alopecia/drug therapy , Minoxidil/administration & dosage , Vasodilator Agents/administration & dosage , Administration, Topical , Adult , Dose-Response Relationship, Drug , Drug Resistance/drug effects , Female , Humans
11.
J Biol Regul Homeost Agents ; 30(1): 131-4, 2016.
Article in English | MEDLINE | ID: mdl-27049083

ABSTRACT

Topical minoxidil is the only drug approved by the US FDA for the treatment of female pattern hair loss. Unfortunately, following 16 weeks of daily application, less than 40% of patients regrow hair. Several studies have demonstrated that sulfotransferase enzyme activity in plucked hair follicles predicts topical minoxidil response in female pattern hair loss patients. However, due to patients’ discomfort with the procedure, and the time required to perform the enzymatic assay it would be ideal to develop a rapid, non-invasive test for sulfotransferase enzyme activity. Minoxidil is a pro-drug converted to its active form, minoxidil sulfate, by sulfotransferase enzymes in the outer root sheath of hair. Minoxidil sulfate is the active form required for both the promotion of hair regrowth and the vasodilatory effects of minoxidil. We thus hypothesized that laser Doppler velocimetry measurement of scalp blood perfusion subsequent to the application of topical minoxidil would correlate with sulfotransferase enzyme activity in plucked hair follicles. In this study, plucked hair follicles from female pattern hair loss patients were analyzed for sulfotransferase enzyme activity. Additionally, laser Doppler velocimetry was used to measure the change in scalp perfusion at 15, 30, 45, and 60 minutes, after the application of minoxidil. In agreement with our hypothesis, we discovered a correlation (r=1.0) between the change in scalp perfusion within 60 minutes after topical minoxidil application and sulfotransferase enzyme activity in plucked hairs. To our knowledge, this is the first study demonstrating the feasibility of using laser Doppler imaging as a rapid, non-invasive diagnostic test to predict topical minoxidil response in the treatment of female pattern hair loss.


Subject(s)
Alopecia/drug therapy , Laser-Doppler Flowmetry , Minoxidil/administration & dosage , Minoxidil/therapeutic use , Administration, Topical , Female , Humans
12.
Int J Clin Pract ; 70(1): 66-81, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26662296

ABSTRACT

OBJECTIVES: This study examined potential benefits of diagnosing and treating elderly adults with overactive bladder (OAB) symptoms. METHODS: Data were analysed from the OAB Re-Contact Study (N = 2750), a cross-sectional, self-reported Internet survey. Elderly respondents (65+ years old) with OAB were identified according to current medication use to control OAB symptoms or by scores > 14 (men) or > 16 (women) on the OAB Awareness Tool. Treated were those currently using prescription medication and never treated were those who never used prescription medication for OAB. Outcome measures included health-related quality of life, activity impairment, OAB-related severity and symptoms, and healthcare resource use (e.g. hospitalisations). Generalised linear models predicted health outcomes as a function of diagnosis or treatment, adjusting for covariates. RESULTS: Diagnosed vs. not diagnosed elderly respondents had higher mental component summary (MCS) scores and SF-6D health utilities, and less activity impairment. Treated vs. never treated elderly respondents had higher MCS and SF-6D health utilities, less activity impairment, fewer OAB symptoms, lower OAB Awareness Tool scores, and lower odds of having bladder problems or incontinence. There were no significant differences in healthcare resource use. Further analysis by age group (middle-aged vs. elderly respondents) revealed significantly greater diagnosis- and treatment-related benefits on MCS (2.93 and 4.49 points more, respectively) and activity impairment (1.24 and 1.37 times as much, respectively) among elderly respondents. CONCLUSIONS: Diagnosis and treatment were each associated with a lower health burden for elderly adults with OAB symptoms. These findings highlighted the importance of diagnosis and treatment in alleviating OAB symptoms and their impact on health outcomes.


Subject(s)
Health Resources/statistics & numerical data , Quality of Life , Urinary Bladder, Overactive/diagnosis , Urinary Bladder, Overactive/drug therapy , Age Factors , Aged , Cross-Sectional Studies , Female , Health Knowledge, Attitudes, Practice , Humans , Male , Middle Aged , Severity of Illness Index
20.
Int J Clin Pract ; 69(9): 1015-28, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26136208

ABSTRACT

OBJECTIVE: Tobacco, widely used in China, poses a major risk for chronic obstructive pulmonary disease (COPD). This study assessed health outcomes of COPD-diagnosed smokers vs. never smokers and examined treatment patterns of patients attempting to quit smoking in urban China. METHODS: National Health and Wellness Survey (NHWS) 2010 and 2012 China data were analysed. Respondents self-reporting diagnosis with COPD, chronic bronchitis, or emphysema were categorised: quit attempters (current smokers 'trying to quit' or non-smokers 'in the process of quitting'), smokers (including quit attempters) and those who never smoked. Respondents reported smoking cessation treatment utilisation; health status: SF-36v2-based scores and SF-6D health utilities; Work Productivity and Activity Impairment questionnaire-based metrics; and resource utilisation. Regression modelling assessed health outcomes, controlling for covariates. RESULTS: Among 1421 (3.6%) diagnosed respondents, 51.6% never smoked and 35.5% smoked (of whom, 43.8% were attempting to quit). After adjustments, smokers vs. never smokers had significantly lower health utilities, lower mental/physical health status and greater absenteeism, presenteeism, overall work impairment, activity impairment, emergency room visits, hospitalisations and provider visits. Quit attempters were diagnosed an average 6.9 years (SD = 7.7) previously, with 25.3% reporting moderate/severe COPD. Most-reported main causes of COPD were: smoking (57.5%), illnesses/conditions (53.8%) and pollutants (44.3%). Among quit attempters, 82.8% smoked currently. Use of prescription cessation treatments was reported by 12.7%. CONCLUSIONS: Smokers experienced poorer health outcomes, reinforcing importance of prevention in mitigating disease burden. Among quit attempters, few reported using prescription cessation treatments. Given the high burden imposed by smoking in China, effective interventions may be beneficial.


Subject(s)
Bronchitis, Chronic/epidemiology , Pulmonary Disease, Chronic Obstructive/epidemiology , Pulmonary Emphysema/epidemiology , Smoking/epidemiology , Absenteeism , Adult , Aged , China/epidemiology , Cost of Illness , Female , Health Services/statistics & numerical data , Health Status , Hospitalization , Humans , Male , Middle Aged , Quality of Life , Regression Analysis , Smoking/adverse effects , Urban Population/statistics & numerical data
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