Infections in human?s results from a variety of disease-causing agents or so-called microorganisms like bacteria, viruses, fungi, viroids or nematodes. Generally, these microorganisms produce endotoxins and exotoxins when they enter the human body. Consequently, the human body reacts by initiating a
Bioinformatic analysis and pharmacological properties of porphyrine and some of its derivatives
Infections in human’s results from a variety of disease-causing agents or so-called microorganisms like bacteria, viruses, fungi, viroids or nematodes. Generally, these microorganisms produce endotoxins and exotoxins when they enter the human body. Consequently, the human body reacts by initiating an inflammatory response that can be “in some cases” very dangerous and lethal. With the current changes in food intake habits and environmental exposures, human cells are often exposed to wide array of microbial infections. Among such microbes, Helicobacter pylori and Pseudomonas aeruginosa are the most infectious, causing moderate to severe abnormalities in human health. Although, there are numerous assay based and standardized procedures and strategies to diagnose these infection, however, with advent of recent advances in spectroscopic methods can be more sensitive and robust. The proposed research study is based on using reflectance spectroscopy (FTIR-ATR, NIR) techniques to detect the presence of infections in clinical samples. This method is based on detecting different microbial toxins. The type III secreted toxins of Pseudomonas aeruginosa are important virulence factors associated with clinically important infection. H. pylori has multiple virulence factors that participate in the pathogenesis of the disease. The new method will have a great impact on the healt sciences showing no clear symptoms and so might be lethal. Currently, the presence of infections is tested by different methods such as clinical sample cultures and other specific antibody tests, the results take approximately 5-15 days to be revealed. Long analysis time may cause delayed therapy leading to many other health complications. Our new developing method will be able to detect the presence of an infection in a shorter time compared to the currently used methods. Also, different types of microorganisms may be specified in our method. The early detection of many infections leads to better treatment outcomes and prevents many complications associated with these infections.
The long-term objectives of this study will be:
To validate the proposed method with the available methods of diagnosis by using molecular and kit based approaches.
| A 1.1. Collection and storage of clinical samples A.1.2. Literature review of the applications of Near-Infrared spectroscopic techniques to the analysis of clinical samples. Literature review of statistical methods applied for the analysis of physiochemical properties of clinical samples. Literature review of multivariate classification methods related to samples and authenticity. |
| A.1.3. Analysis of clinical samples and collection of spectral data by using FTNIR & FTIR |
| A. 1.4. Spectral pre-treatment (preprocessing) |
| A.1.5. Determination of physiochemical properties of clinical samples from spectral data base |
| A. 1.5.1. Development of PCA & PLSDA models |
| A. 2.1. To explore the similarities and diffence among the healthy and infected clinical samples |
| A 2.2. To determine a specific infection |
| A 2.3. To investigate the strength or level of the infection |
| A.1.2. Literature review of the applications of Near-Infrared spectroscopic techniques to the analysis of clinical samples. Literature review of statistical methods applied for the analysis of physiochemical properties of clinical samples. Literature review of multivariate classification methods related to samples and authenticity. |
| A.1.3. Analysis of clinical samples and collection of spectral data by using FTNIR & FTIR |
| A. 1.4. Spectral pre-treatment (preprocessing) |
| A.1.5. Determination of physiochemical properties of clinical samples from spectral data base |
| A. 1.5.1. Development of PCA & PLSDA models |
| A. 2.1. To explore the similarities and diffence among the healthy and infected clinical samples |
| A 2.2. To determine a specific infection |
| A 2.3. To investigate the strength or level of the infection |
| A.1.2. Literature review of the applications of Near-Infrared spectroscopic techniques to the analysis of clinical samples. Literature review of statistical methods applied for the analysis of physiochemical properties of clinical samples. Literature review of multivariate classification methods related to samples and authenticity. |
| A.1.3. Analysis of clinical samples and collection of spectral data by using FTNIR & FTIR |
| A. 1.4. Spectral pre-treatment (preprocessing) |
| A.1.5. Determination of physiochemical properties of clinical samples from spectral data base |
| A. 1.5.1. Development of PCA & PLSDA models |
| A. 2.1. To explore the similarities and diffence among the healthy and infected clinical samples |
| A 2.2. To determine a specific infection |
| A 2.3. To investigate the strength or level of the infection |
A 1.1. Collection and storage of clinical samples
A.1.2. Literature review of the applications of Near-Infrared spectroscopic techniques to the analysis of clinical samples. Literature review of statistical methods applied for the analysis of physiochemical properties of clinical samples. Literature review of multivariate classification methods related to samples and authenticity.
A.1.3. Analysis of clinical samples and collection of spectral data by using FTNIR & FTIR
A. 1.4. Spectral pre-treatment (preprocessing)
A.1.5. Determination of physiochemical properties of clinical samples from spectral data base
A. 1.5.1. Development of PCA & PLSDA models
A. 2.1. To explore the similarities and diffence among the healthy and infected clinical samples
A 2.2. To determine a specific infection
A 2.3. To investigate the strength or level of the infection
A.1.2. Literature review of the applications of Near-Infrared spectroscopic techniques to the analysis of clinical samples. Literature review of statistical methods applied for the analysis of physiochemical properties of clinical samples. Literature review of multivariate classification methods related to samples and authenticity.
A.1.3. Analysis of clinical samples and collection of spectral data by using FTNIR & FTIR
A. 1.4. Spectral pre-treatment (preprocessing)
A.1.5. Determination of physiochemical properties of clinical samples from spectral data base
A. 1.5.1. Development of PCA & PLSDA models
A. 2.1. To explore the similarities and diffence among the healthy and infected clinical samples
A 2.2. To determine a specific infection
A 2.3. To investigate the strength or level of the infection
A.1.2. Literature review of the applications of Near-Infrared spectroscopic techniques to the analysis of clinical samples. Literature review of statistical methods applied for the analysis of physiochemical properties of clinical samples. Literature review of multivariate classification methods related to samples and authenticity.
A.1.3. Analysis of clinical samples and collection of spectral data by using FTNIR & FTIR
A. 1.4. Spectral pre-treatment (preprocessing)
A.1.5. Determination of physiochemical properties of clinical samples from spectral data base
A. 1.5.1. Development of PCA & PLSDA models
A. 2.1. To explore the similarities and diffence among the healthy and infected clinical samples
A 2.2. To determine a specific infection
A 2.3. To investigate the strength or level of the infection
This study will introduce a new and robust method to detect and characterize the presence of infection in clinical samples. This will have a great impact on the early treatment plan as it will improve the therapeutic outcomes and eliminate complications related to the delayed therapeutic interventions.
The delayed diagnostic tools results for infectious diseases like common infectious diseases, such as Tuberculosis (TB), Dengue fever, diabetics, Malaria have a negative impact on patient’s health, may lead to other complications and even death in some cases, therefore, application of reflectance spectroscopy both FTIR & NIR coupled with multivariate methods as a robust diagnostic tool for clinical blood samples.
| Elapsed time in (days or weeks or month or quarter) since start of the project | Milestone | Deliverable |
|---|---|---|
| Month 1 | A 1.1. Collection and storage of clinical samples. | 6 |
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