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Home > Synthesis, Characterization and Modification of Gum Arabic Microgels for Biomedical and Environmental Applications

Synthesis, Characterization and Modification of Gum Arabic Microgels for Biomedical and Environmental Applications

Thesis Info

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Author

Farooq, Muhammad

Program

PhD

Institute

Quaid-I-Azam University

City

Islamabad

Province

Islamabad.

Country

Pakistan

Thesis Completing Year

2018

Thesis Completion Status

Completed

Subject

Chemistry

Language

English

Link

http://prr.hec.gov.pk/jspui/bitstream/123456789/9178/1/Muhammad_Farooq_Chemistry_HSR_2018_QAU_21.06.2018.pdf

Added

2021-02-17 19:49:13

Modified

2024-03-24 20:25:49

ARI ID

1676727517086

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In this study, Gum Arabic (GA) microgels were successfully synthesized via reverse micellization method with a high yield (78±5.0%) in 5-100 μm size range using divinyl sulfone (DVS) as a crosslinker. The as synthesized GA microgels show 22.8±3.5% biodegradability property at stomach condition (pH 1) in 20 days, whereas no degradation was observed at pH 7.4 and pH 9 conditions at 37 oC. By using diethylenetriamine (DETA) and taurine (TA) as chemical modifying agents, GA microgels were chemically modified as GA-DETA and GA-TA microgels. Remarkably, GA-DETA and GA-TA microgels show zeta potential values of 5.23±4.07 and -24.85±1.33 mV in comparison to GA microgels which give -27.31±4.20 mV overall surface charge. Moreover, blood compatibility of GA, GA-TA, and GA-DETA microgels was tested via in vitro protein adsorption, % hemolysis ratio and blood clotting index. Interestingly, GA based microgels were hemocompatible with % hemolysis ratio between 0.23 and 2.05; and the GA microgels were found highly compatible with a blood clotting index of 81±40. The biocompatibility of GA, GA-DETA and GA-TA microgels against L929 fibroblast cells also indicate 84.4%, 89.1% and 67.0% cell viability respectively at 25.0 μg/mL concentration; suggesting a great deal of potential in vivo biomedical applications up to this concentration. In addition, 5 and 10 mg/mL minimum inhibition concentration (MIC) of protonated GA-DETA microgels (GA-DETA-HCl) was determined against E. coli and S. aureus respectively. The bare and GA-TA microgels present good loading capability of 160 and 57 mg.g-1 for phenylephrine (PHP) whereas, in case of Trimethoprim(TMP), GA-DETA and GA-TA microgels show a relatively higher loading capacity of 80 and 52 mg.g-1 respectively. Contrarily, 39.27 ±1.20, 18.40 ±3.130 and 3.10 ±1.140 mg.g-1 release of PHP was observed in case of GA, GA-TA and GA-DETA microgels respectively to the BPS medium in 8 Hrs. Likewise, GA and GA-TA microgels exhibits upto 4.5 ±3.32 and 9.80 ±4.10 mg.g-1 release respectively and an unexpectedly low release amount of 3.3 ±1.94 mg.g-1 from GA-DETA microgels was monitored in case of TMP. Besides, Zeta potential measurements in this study suggest that GA-DETA microgels denote a positively charged surface in DI water. Due to this fact, GA-DETA microgels were used as micro reactor in removal study of some negatively charged pollutants such as; chromate(Cr(III)), dichromate(Cr(VI)), arsenate(As(V)), methyl orange(MO), eosin Y(EY) and Congo red(CR) from aqueous media. Thus, 0.05 g feed of GA-DETA microgels show upto 69.80, 99.30 %, 40.0 %, 91.0%, 84.10 % and 73.0 % removal capability for As(V), Cr(VI), Cr(III), MO, EY and CR respectively in 2 Hrs. mixing time. Moreover, kinetic models such as; the Langmuir, the Fruendlich and modified Fruendlich isotherms were applied to the obtained adsorption data and it was concluded that modified Fruendlich model exhibits relatively practical fit for almost all pollutants giving R2 value nearer to unity. Moreover, maximum adsorption capacity (Qm) was determined for all the six pollutants with the numerical values of 217, 256, 271, 143, 130 and 116 mg.g-1 for As (V) Cr(III), Cr(VI), MO, EY and CR respectively. Further, it was observed that the modified Fruendlich isotherm give inclusively best fit for all pollutants showing R2 values of 0.9962, 0.9926, 0.9972, 0.9988, 0.9988 and 0.980 in case of adsorption As(V), Cr(VI), Cr(III), MO, EY and CR respectively.
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فرقت

فرقت

دل رو رو وقت گزار گیا
غم یار دا سانوں مار گیا

جدوں ماہی دے کول وسدے سی
دکھ ویکھ اسانوں نسدے سی
لوکی روندے تے اسیں ہسدے سی
کوئی دشمن دا چل وار گیا

دل یار نوں ڈھونڈن چلیا اے
کر وعدہ یار نہ ولیا اے
میرے دل وچ بھانبھڑ بلیا اے
تیر شوق دا ہو ہن پار گیا

دل یار بناء ہون رہندا نئیں
اے درد ہجر دے سہندا نئیں
دکھ درد کسے نوں اے کہندا نئیں
سکھ چین تے نال قرار گیا

عشق دے روگوں رب بچائے
یار بنا ہن چین نہ آئے
شوق سجن دا ودھدا جائے
کیوں سوہنا یار وسار گیا

قادری سائیںؔ عشق بازار نہ جاویں
جاویں تاں سچا عشق کماویں
ہک دن درشن یار دا پاویں
سوہنا ملے تاں دکھ ہزار گیا

Socio-Economic Factors of Differences in Public Health-Related Variables among Women: A Cross-Sectional Study

This study examines the association of living areas (slum and non-slum) with the selected public health-related variables in the presence of socioeconomic variables among married women and also having a child. A total of 150 women aged 18 to 49 are selected of which 50 women from slums and 100 women are from non-slum areas of Multan by applying the cluster and random sampling techniques. The cross-tabulation method is used to find the results. The dependent variable is Body Mass Index (BMI) and it is analyzed with the socio-economic variables such as mass media index, household characteristics and education. The findings exhibit that the BMI of the women living in the slum areas is low due to a low level of education, lack of mass media access, bad household structures, and poor or ignorant area. The women of the slum area have fewer mass media access, poor status of household characteristics and less education as compared to the women living in the non-slum areas. BMI is significantly affected by area, women's education and household characteristics except for physical work, job status, mass media access and husband education. The findings of this study suggest that to provide health facilities or to reduce the gap in public health, education, mass media access and households characteristics might be considered while making any decision related to the slum and non-slum areas.

Optimization of Factors Affecting Biodegradation of Chlorpyrifos in Soil and Water Environments

Chlorpyrifos an insecticide, is extensively used in Pakistan and contaminating the soil and water environments at several sites. Exploration of efficient chlorpyrifos-degrading bacteria to clean-up this toxicant is of immense importance. This study reports the isolation, screening and identification of highly efficient chlorpyrifos degrading bacterial strains from different soils and water samples collected from different sites of Pakistan. Out of total 50 isolated bacterial strains, 32 were tested for their biodegradation capability in a culture medium containing chlorpyrifos as carbon and energy source. The bacterial isolates showed a great variation (25-92%) in their ability to degrade chlorpyrifos in broth condition. Out of these 32 strains, four bacterial strains (SWLC2, SWLH2, SGB2 and SWLC1) were the most promising in their growth and biodegradation activity and were identified and characterized by biochemical characteristics and 16S rRNA sequence analyses. Three strains (SGB2, SWLC1 and SWLC2) showed the greatest similarity to the members of Enterobacteriacea and one strain (SWLH2) to Rhizobiacea families. These selected strains (Enterobacter sp. SWLC1, Enterobacter sp. SGB2, Agrobacterium sp. SWLH2 and Enterobacter sp. SWLC2) exhibited biodegradation potential between 81 to 92% of the spiked amount of chlorpyrifos (100 mg l -1 ) within 18 days of incubation in broth culture. Biodegradation of chlorpyrifos continued gradually throughout the incubation period (18 days) as examined by the HPLC - UV system. Abiotic degradation contributed only up to 15% of the spiked amount. Maximum biodegradation by the four efficient bacterial strains was observed at an initial pH of 7 and an incubation temperature of 30 o C, under shaking conditions. Among these four strains, Enterobacter sp. SWLC2 was found most efficient in biodegradation of chlorpyrifos and was selected for further studies. This strain was then optimized in broth as well as in soil slurry under different conditions. Enterobacter sp. SWLC2 showed maximum biodegradation of chlorpyrifos at pH 7, 30 o C, under shaking conditions with inoculum size of 800 μl. Biodegradation of chlorpyrifos by Enterobacter sp. SWLC2 varied in different textured soils, being more rapid in course textured soils than in fine textured soil. Among these soils, loamy soil was selected for further studies in soil slurry experiments due to its medium textured nature as soils of Punjab are mostly loamy in texture. An initial inoculum size of 800 μl (OD= 0.80), incubation temperature of 30 o C, under shaking, initial pH 7 of soil slurry of loam soil were found optimal conditions for maximum biodegradation of chlorpyrifos byEnterobacter sp. SWLC2. Exogenous application of sugars, yeast extract, manitol, organic acids and amino acids had stimulator or inhibitory effects on biodegradation of chlorpyrifos by Enterobacter sp. SWLC2. Among these, glucose, yeast extract, succinic acid and citric acid had stimulatory effects on biodegradation of chlorpyrifos. Biodegradation of chlorpyrifos by Enterobacter sp. SWLC2 was also checked at different initial concentrations of chlorpyrifos from 10-250 mg l -1 . Rate of biodegradation increased with increase in concentration of chlorpyrifos from 100-150 mg l -1 and suggested first order rate kinetics. In all experiments, utilization of chlorpyrifos by the strains was accompanied by a parallel increase in optical densities of broth implying that removal of this pesticide from the growth medium was a growth linked biodegradation. These results highlighted the potential of this bacterium to be used in the detoxification strategies of chlorpyrifos contaminated water and soil environments.