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<title>SCHOOL OF PHYSICAL SCIENCES</title>
<link href="http://hdl.handle.net/123456789/952" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/123456789/952</id>
<updated>2026-04-14T23:14:16Z</updated>
<dc:date>2026-04-14T23:14:16Z</dc:date>
<entry>
<title>Drug Delivery by Zeolite Nanomaterials in Treatment of Breast Cancer: In Vitro</title>
<link href="http://hdl.handle.net/123456789/12221" rel="alternate"/>
<author>
<name>Nyarko, Savanna</name>
</author>
<id>http://hdl.handle.net/123456789/12221</id>
<updated>2025-06-09T11:58:43Z</updated>
<published>2024-01-01T00:00:00Z</published>
<summary type="text">Drug Delivery by Zeolite Nanomaterials in Treatment of Breast Cancer: In Vitro
Nyarko, Savanna
In this work, synthetic Linde type A (LTA) zeolites were examined to find out how well they could encapsulate and release doxorubicin cancer drug. Synthetic zeolites were used for this study because of their uniform pore distribution and crystal purity. The samples were characterized using X-ray diffraction spectroscopy (XRD) and Fourier Transform Infrared Spectroscopy (FTIR). The XRD data on the control LTA zeolite showed average crystallite size of 40.89 nm, 28.40 nm and 29.76 nm at 60℃, 80 ℃ and 105 ℃ respectively. The percentage crystallinity also revealed values of 65.99, 71.39 and 76.37 at 60℃, 80 ℃ and 105 ℃ respectively. The XRD diffraction pattern on drug loaded LTA zeolite showed average crystallite size of 24.89 nm, 16.44 nm and 26.91 nm at 60℃, 80 ℃ and 105 ℃ respectively. The percentage crystallinity of the loaded drug on LTA zeolite also revealed values of 70.79, 83.78 and 68.82 at 60℃, 80 ℃ and 105 ℃ respectively. The FTIR data also showed the signature peaks characteristics of LTA zeolites at all the three temperatures (60℃, 80 ℃ and 105 ℃). The morphology of the control and loaded LTA zeolites were determined by Helium Ion Microscope (HIM) and Scanning Electron Microscope (SEM). Brunauer-Emmett- Teller (BET) surface area, pore size and pore volume were also determined. The drug release data from 60 ℃ had a correlation (R2) values of 0.9139, 0.8764 and 0.7844 with the first-order, Hixson-Crowell and zero-order models respectively. Drug release data for 80 ℃ and 105 ℃ also had a (R2) values of 0.7345 and 0.5160 respectively for the Korsmeyer-Peppas model. The Alamar blue assay cell viability results showed that 105 ℃ was cytotoxic to the cells with an IC50 of 92 μg/ml.
xiii, 100p:, ill.
</summary>
<dc:date>2024-01-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Quartic Rank Transmutation of Gamma–Type Distributions: Characteristics and Estimation</title>
<link href="http://hdl.handle.net/123456789/12219" rel="alternate"/>
<author>
<name>Manu, Jones Asante</name>
</author>
<id>http://hdl.handle.net/123456789/12219</id>
<updated>2025-06-09T11:46:51Z</updated>
<published>2023-12-01T00:00:00Z</published>
<summary type="text">Quartic Rank Transmutation of Gamma–Type Distributions: Characteristics and Estimation
Manu, Jones Asante
Rank transmutation maps have emerged as one of the adopted methods for&#13;
proposing new probability distributions. This study used the quartic rank transmutation&#13;
to introduce three new probability distributions: the Quartic Transmuted&#13;
Exponential Distribution, Quartic Transmuted Lindley Distribution, and&#13;
Quartic Transmuted Rayleigh Distribution. The construction of these distributions&#13;
involves meticulously examining mathematical concepts, encompassing&#13;
probability density functions, survival functions, moments, entropies, and order&#13;
statistics. Visual aids, including cumulative distribution functions, probability&#13;
density functions, and hazard rate functions, enhance the comprehension&#13;
of distribution characteristics. A comprehensive simulation study underscores&#13;
a consistent trend: a reduction in bias for maximum likelihood estimation and&#13;
refinement in standard errors with increasing sample size. The practical applicability&#13;
of these newly proposed distributions was demonstrated using real-world&#13;
datasets. The quartic transmuted exponential distribution was effectively employed&#13;
to model the lifetime of 50 devices, referencing data from Aarset’s study&#13;
in 1987. Similarly, the quartic transmuted Lindley distribution was adeptly applied&#13;
to remission times (measured in months) of 128 bladder cancer patients.&#13;
Finally, the quartic transmuted Rayleigh distribution was successfully utilized&#13;
to analyze a dataset comprising 72 instances of exceedance from the Wheaton&#13;
River flood data near Carcoss in Yukon Territory, Canada. Evaluation criteria&#13;
such as log-likelihood, AIC, AICc, and BIC affirm the superior flexibility&#13;
and performance of the proposed distributions. This research significantly contributes&#13;
to distribution theory, offering innovative methods to enhance distribution&#13;
adaptability in diverse applications.
xi, 171p:, ill.
</summary>
<dc:date>2023-12-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Analysis of Levels of Heavy Metals, Essential Elements and Persistent Organic Pollutants (Pops) in Human Breast Milk: A Study at the Ho Teaching Hospital</title>
<link href="http://hdl.handle.net/123456789/12212" rel="alternate"/>
<author>
<name>Amstrong, Justice Wiston  Jonathan</name>
</author>
<id>http://hdl.handle.net/123456789/12212</id>
<updated>2025-06-09T10:48:48Z</updated>
<published>2023-02-01T00:00:00Z</published>
<summary type="text">Analysis of Levels of Heavy Metals, Essential Elements and Persistent Organic Pollutants (Pops) in Human Breast Milk: A Study at the Ho Teaching Hospital
Amstrong, Justice Wiston  Jonathan
Human breast milk is, by far, the richest source of nutrition. However, breast milk is not pristine. The study aimed to analyse breast milk at lactational stages for persistent organic pollutants (OCPs, PCBs and PFAS), five heavy metals and essential elements. Participants for the study were healthy lactating mothers (aged 18 – 42 years) from first to third week postpartum. Forty-seven participants were recruited for the study. Forty millilitres (40 mL) of colostrum, transitional milk and mature milk were collected from each participant, making a total of 150 samples. Besides, each participant completed a comprehensive questionnaire to elicit information on biodata, place of residence and dietary pattern. Ten millilitres (10 mL) aliquot of each breast milk sample was prepared, extracted and analysed for PFAS using UPLC–MS/MS. Another 10 mL aliquot sample was extracted using QUECHERS and cleaned up and analysed for OCPs and PCBs using GC – ECD and GC–MS respectively A further 10 mL aliquots sample were acid digested employing EPA Method 3010A and analysed using ICP-OES. Statistical analyses were performed using IBM SPSS (Version 24), Excel Tool Pak and XLSTAT 2022.4.1.1377 and the results summarised in tables and figures. The mean Levels and ranges of PFAS detected in breast milk ranged from 2.65 ± 3.31 ng/L (PFHxA) – 83.14 ± 38.61 ng/L (PFOS). Both OCPs and PCBs analyzed were all below limits of detection. Mean levels of heavy metals in colostrum, transitional milk and mature milk respectively ranged from 0.002 (Cd) – 0.872 (Al) μg/L; 0.002 (Cd) – 0.997 (Pb) μg/L and 0.002 (Cd) – 0.564 (Al). The mean levels of essential elements ranged from 0.07 (Se) – 815.00 (K); 0.07 (Se) – 1008,00 (Na) and 0.07 (Se) – 596.00 (K) respectively during the stages of lactation.
xxxii, 430p:, ill.
</summary>
<dc:date>2023-02-01T00:00:00Z</dc:date>
</entry>
<entry>
<title>Mathematical Model of Immune Response to Hepatitis B Virus and Liver Cancer Co-Existence Dynamics in the Presence of Treatment</title>
<link href="http://hdl.handle.net/123456789/12200" rel="alternate"/>
<author>
<name>Chataa, Paul</name>
</author>
<id>http://hdl.handle.net/123456789/12200</id>
<updated>2025-06-05T13:41:45Z</updated>
<published>2024-07-01T00:00:00Z</published>
<summary type="text">Mathematical Model of Immune Response to Hepatitis B Virus and Liver Cancer Co-Existence Dynamics in the Presence of Treatment
Chataa, Paul
The principal method for modeling the spread of infectious diseases generally involves&#13;
the application of ordinary differential equations. Studies have demonstrated&#13;
that an effective strategy for refining certain mathematical models is the integration&#13;
of fractional-order differential equations. To gain a more profound understanding of&#13;
the interactions between the hepatitis B virus (HBV), liver cancer, and immune system&#13;
cells, a mathematical model that combined both ordinary and fractional differential&#13;
equations was investigated. This model was closely aligned with experimental&#13;
data on viral DNA load. The work concentrated on four qualitative scenarios: the&#13;
innate immune response, adaptive immune response, cytokine response, and the coexistence&#13;
of infection dynamics. Unlike earlier models, liver cells were classified&#13;
into distinct stages of infection. For populations of non-pathogenic macrophages in&#13;
the presence and absence of malignant cells, the study calculated the invasion probability&#13;
for transmission dynamics, represented by the control reproduction number,&#13;
Rc. The iterated two-step Adams-Bashforth method was employed for numerical&#13;
simulations using the ABC fractional derivative in the Caputo sense, while the Latin&#13;
Hypercube Sampling (LHS) and Partial Rank Correlation Coefficients (PRCC) techniques&#13;
were utilized for parameter sensitivity analysis. The work identified the key&#13;
transmission mechanism of viral load and proposed an optimal therapeutic method&#13;
for viral treatment. Model parameters were estimated using nonlinear least squares&#13;
fitting of longitudinal data (serum HBV DNA viral load) from existing literature.&#13;
Finally, the study compared the classical-order model system with the ABC fractional&#13;
differential equations model system to determine which offered superior performance.&#13;
Both methods were evaluated using simulation results of the state variables,&#13;
revealing that the fractional model provides more detailed results than the&#13;
classical model.
xvi, 226p:, ill.
</summary>
<dc:date>2024-07-01T00:00:00Z</dc:date>
</entry>
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