Investigation of the interaction of levofloxacin hemihydrate with surfactants in the occurrence of salts: Conductivity and cloud point measurement

Conductometric and cloud point (CP) measurement techniques have been employed in order to investigate the interaction of antibiotic drug levofloxacin hemihydrate (LFH) with anionic surfactant, sodium dodecyl sulfate (SDS) as well as a non-ionic surfactant Tween-80 (Tw-80; polyethylene sorbitol ester) in the absence/occurrence of various salts over the temperature range 298.15–318.15 K keeping regular interval of 5 K. Two clear c* values were extracted for pure SDS along with (SDS + LFH) mixtures where the increase and decrease of c* values due to the addition of LFH and salts respectively demonstrated the happened interaction among the studied components where salts provided a convenient environment for aggregation of surfactants. Negative ∆G°m values of SDS in H2O/(SDS + LFH) mixtures revealed the spontaneous assembling of surfactant molecules and the stability of the aggregates. The values of ∆H°m and ∆S°m indicate the existence of hydrophobic & electrostatic interactions between drug (LFH) and surfactant (SDS). Enthalpy and entropy contributions on the standard free energy of micellization were also calculated. The CP magnitudes of Tween-80 were reduced with increasing its concentration. The occurrence of LFH/(LFH + salts) boosted to lessening the CP values. The positive ∆G°c values suggested the non-spontaneity of clouding while the obtained ∆H°c and ∆S°c values of this CP study demonstrated the two significant accelerating impacts (electrostatic/hydrophobic interactions) between LFH & Tw-80. The thermodynamic properties of transfer for both techniques were also evaluated and analyzed in detail in the current study

Influences of NaCl and Na₂SO₄ on the Micellization Behavior of the Mixture of Cetylpyridinium Chloride + Polyvinyl Pyrrolidone at Several Temperatures

Herein, the conductivity measurement technique is used to determine the interactions that may occur between polyvinyl pyrrolidone (PVP) polymer and cetylpyridinium chloride (CPC) surfactant in the presence of NaCl and Na2SO4 of fixed concentration at variable temperatures (298.15–323.15 K) with an interval of 5 K. In the absence or presence of salts, we observed three critical micelle concentrations (CMC) for the CPC + PVP mixture. In all situations, CMC1 values of CPC + PVP system were found to be higher in water than in attendance of salts (NaCl and Na2SO4). Temperature and additives have the tendency to affect counterion binding values. Various physico-chemical parameters were analyzed and demonstrated smoothly, including free energy (ΔG0m), enthalpy (ΔH0m) and entropy change (ΔS0m). The micellization process is achieved to be spontaneous based on the obtained negative ΔG0m values. The linearity of the ΔHmo and ΔSmo values is excellent. The intrinsic enthalpy gain (ΔH0*m) and compensation temperature (Tc) were calculated and discussed with logical points. Interactions of polymer hydrophobic chains or the polymer + surfactant associated with amphiphilic surface-active drugs can employ a strong impact on the behavior of the gels

Effect of temperature and salt/alcohol on the interaction of tetradecyltrimethylammonium bromide/Triton X-100 with moxifloxacin hydrochloride: A multitechnique approach

Interaction of moxifloxacin hydrochloride (MFH) with tetradecyltrimethylammonium bromide (TTAB) along with Triton X-100 (TX-100) under different experimental conditions has been carried out using multiple physico-chemical techniques. The micellar parameters like critical micelle concentration (cmc), counter ion binding (β), thermodynamic parameters such as ΔGm0, ΔHm0, and ΔSm0etc. associated with the drug-TTAB interaction have been determined. The changes of the values of cmc of TTAB by the addition of drug indicate the existence of TTAB-MFH interaction. The cmc values of drug-TTAB systems were found to be dependent on the variation of temperature, salt and alcohol concentrations. In all the cases the negative values of ΔGm0 indicated the spontaneous micelle formation of drug-TTAB system. The values of ΔHm0 and ΔSm0 reveal the existence of hydrophobic and electrostatic interactions between drug and TTAB. The CP values of TX-100 in water were increased in the presence of MFH. The values of ΔGc0 of drug-TX-100 mixed system are found to be positive which indicates the clouding process is nonspontaneous in nature. The binding constant (Kb) value for MFH-TX-100 system was found to be temperature dependent and the binding interaction between MFH and TX-100 is mainly due to hydrogen bonding.</p

Facile extraction and characterization of calcium hydroxide from paper mill waste sludge of Bangladesh

Herein, paper mill waste sludge (PMS) from two different sources has been investigated to extract calcium hydroxide, Ca(OH)2 by a facile and inexpensive extraction process. PMS samples, collected from local paper mill plants of Bangladesh, were the main precursors wherein HCl and NaOH were used for chemical treatment. The as-synthesized products were analysed by a variety of characterization tools including X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Raman spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) elemental analyses. Our studies confirm that the extracted product contains Ca(OH)2 as a major content, albeit it also includes CaCO3 phase owing to the inescapable carbonation process from the surrounding environment. The particle size of the synthesized products is in the range of 450–500 nm estimated from SEM micrographs. The crystallite domain size of the same estimated from XRD analyses and was found to be approximately 47 and 31 nm respectively for product-A and product-B considering major (101) Bragg peak of Ca(OH)2. The yield percentage of the isolated products is about 65% for samples collected from both sources

Population-level risks of alcohol consumption by amount, geography, age, sex, and year: a systematic analysis for the Global Burden of Disease Study 2020

Background The health risks associated with moderate alcohol consumption continue to be debated. Small amounts of alcohol might lower the risk of some health outcomes but increase the risk of others, suggesting that the overall risk depends, in part, on background disease rates, which vary by region, age, sex, and year. Methods For this analysis, we constructed burden-weighted dose-response relative risk curves across 22 health outcomes to estimate the theoretical minimum risk exposure level (TMREL) and non-drinker equivalence (NDE), the consumption level at which the health risk is equivalent to that of a non-drinker, using disease rates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2020 for 21 regions, including 204 countries and territories, by 5-year age group, sex, and year for individuals aged 15-95 years and older from 1990 to 2020. Based on the NDE, we quantified the population consuming harmful amounts of alcohol. Findings The burden-weighted relative risk curves for alcohol use varied by region and age. Among individuals aged 15-39 years in 2020, the TMREL varied between 0 (95% uncertainty interval 0-0) and 0.603 (0.400-1.00) standard drinks per day, and the NDE varied between 0.002 (0-0) and 1.75 (0.698-4.30) standard drinks per day. Among individuals aged 40 years and older, the burden-weighted relative risk curve was J-shaped for all regions, with a 2020 TMREL that ranged from 0.114 (0-0.403) to 1.87 (0.500-3.30) standard drinks per day and an NDE that ranged between 0.193 (0-0.900) and 6.94 (3.40-8.30) standard drinks per day. Among individuals consuming harmful amounts of alcohol in 2020, 59.1% (54.3-65.4) were aged 15-39 years and 76.9% (73.0-81.3) were male. Interpretation There is strong evidence to support recommendations on alcohol consumption varying by age and location. Stronger interventions, particularly those tailored towards younger individuals, are needed to reduce the substantial global health loss attributable to alcohol

Population-level risks of alcohol consumption by amount, geography, age, sex, and year: a systematic analysis for the Global Burden of Disease Study 2020

Background: The health risks associated with moderate alcohol consumption continue to be debated. Small amounts of alcohol might lower the risk of some health outcomes but increase the risk of others, suggesting that the overall risk depends, in part, on background disease rates, which vary by region, age, sex, and year. Methods: For this analysis, we constructed burden-weighted dose–response relative risk curves across 22 health outcomes to estimate the theoretical minimum risk exposure level (TMREL) and non-drinker equivalence (NDE), the consumption level at which the health risk is equivalent to that of a non-drinker, using disease rates from the Global Burden of Diseases, Injuries, and Risk Factors Study (GBD) 2020 for 21 regions, including 204 countries and territories, by 5-year age group, sex, and year for individuals aged 15–95 years and older from 1990 to 2020. Based on the NDE, we quantified the population consuming harmful amounts of alcohol. Findings: The burden-weighted relative risk curves for alcohol use varied by region and age. Among individuals aged 15–39 years in 2020, the TMREL varied between 0 (95% uncertainty interval 0–0) and 0·603 (0·400–1·00) standard drinks per day, and the NDE varied between 0·002 (0–0) and 1·75 (0·698–4·30) standard drinks per day. Among individuals aged 40 years and older, the burden-weighted relative risk curve was J-shaped for all regions, with a 2020 TMREL that ranged from 0·114 (0–0·403) to 1·87 (0·500–3·30) standard drinks per day and an NDE that ranged between 0·193 (0–0·900) and 6·94 (3·40–8·30) standard drinks per day. Among individuals consuming harmful amounts of alcohol in 2020, 59·1% (54·3–65·4) were aged 15–39 years and 76·9% (73·0–81·3) were male. Interpretation: There is strong evidence to support recommendations on alcohol consumption varying by age and location. Stronger interventions, particularly those tailored towards younger individuals, are needed to reduce the substantial global health loss attributable to alcohol. Funding: Bill & Melinda Gates Foundation