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1.
Curr Pharm Des ; 28(3): 208-215, 2022.
Article in English | MEDLINE | ID: mdl-34620072

ABSTRACT

Since the inception of nanotechnology, several efforts have been dedicated to fabricating diverse nanodevices with exceptional performance. These innovative constructs have been applied in medicine due to their tailorable physicochemical properties (chemical composition, optical activity, spectra, and charge) and morphological attributes (size, shape, and surface area). Moreover, these versatile nanomedicines could promisingly offer better performance over the conventional therapeutic strategies. Broadly speaking, in terms of chemical composition, nanobiomaterials are classified into two predominant categories of organic and inorganic- based components. Despite their success and enormous versatile advancements in the past two decades, the significant progress towards clinical translation has been hampered by their corresponding intrinsic limitations. In this perspective, we give a brief overview of these organic- and inorganic-based materials, highlighting opportunities and challenges towards their utilization in medicine. Finally, we provide an interesting outlook on the lessons learned and look forward to further developing these materials, emphasizing their potential in clinical translation.


Subject(s)
Nanomedicine , Nanotechnology , Humans
2.
J Pharm Sci ; 106(5): 1391-1395, 2017 05.
Article in English | MEDLINE | ID: mdl-28130035

ABSTRACT

A relationship between the chenodeoxycholate (CDC) monomer concentration and the total concentration of CDC was established using a kinetic dialysis technique. Meanwhile, the sizes of the formed simple CDC micelles were measured by a quasielastic light-scattering (QLS) technique to be nearly constant. The QLS results led to a suggestion for equilibrium models of CDC aggregate formation. According to the established relationship and the suggested models, the best curve-fitting model was selected by a least-squares technique. Furthermore, the model parameters were quantified. Based on the quantified parameters, at a minimum detectable concentration of simple CDC micelles to be ∼0.2 mM, an appropriate model corresponding concentration of CDC monomers was estimated to be ∼3.08 mM. This value is consistent with a minimum monomer CDC concentration of ∼3.13 mM for simple CDC micelle formation estimated according to the present QLS detection and the model prediction. The consistency confirms the model prediction that at a low CDC monomer concentration (<3 mM), the concentration of stable CDC dimers is much higher than that of simple CDC micelles but the contribution of simple CDC micelles to the total CDC concentration cannot be negligible.


Subject(s)
Chenodeoxycholic Acid/chemistry , Chenodeoxycholic Acid/metabolism , Models, Chemical , Protein Aggregates/physiology , Cathartics/chemistry , Cathartics/metabolism , Forecasting
3.
Microsc Microanal ; 22(6): 1329-1337, 2016 12.
Article in English | MEDLINE | ID: mdl-27890026

ABSTRACT

There is an unmet need for researchers in life sciences and clinical pathology to obtain untainted target cells with very high accuracy, which are suitable for subsequent genome and protein analysis. In this paper, an electrostatic capture laser microdissection technology (ECM) is proposed and explained. Following microscopic identification and separation of target cells from the surrounding tissues using laser cutting, the ECM uses electrostatic forces to capture target cells. Validation experiments indicate that ECM can capture a wide assortment of contamination-free homogeneous samples, ranging from very tiny pieces of a few micrometers in diameter to large pieces with a surface area of over 40,000 µm2. Evidence is also provided indicating that uncontaminated homogeneous tissue materials collected by ECM are suitable for further DNA and RNA analysis. This suggests that ECM capture causes little or no identifiable damage to the collected tissues. This technique has significant advantages compared with existing traditional capture methods, such as very low risk of biological sample damage and the fact that it can be applied to both upright and inverted microscopy. The latter allows for separating target cells in tissue culture. ECM usage provides a cost-effective alternative to more traditional laser capture microdissection techniques.


Subject(s)
Laser Capture Microdissection/methods , DNA/isolation & purification , Lasers , RNA/isolation & purification , Static Electricity
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