Transition metal-ions based nanocomposites are widely used for their ease of synthesis and cost-effectiveness in sensor development. In this study, we have synthesized bi-metallic (iron and zinc) metal organic framework...
Herein, we report the preparation of a metal-chelate immobilized hydrophilic poly hydroxyethylmethacrylate-based monolith of 100 μL volume in a plastic syringe. The monolith is elastic in nature, contains well interconnected pores with a permeability (k) of 1.3 × 10 m . Immobilization of iminodiacetic acid (IDA) is performed via schiff base reaction. Adsortion of IgG on this copper-IDA monolith is of langmuir isotherm with a maximum adsorption capacity of ∼25 mg IgG per g monolith. IgG adsorption capacity of this affinity monolith remained unaffected with increase of flow rate. This proposed metal-chelate monolith in syringe format has the potential for application in proteomics.
Penicillin discovery has put forward great expectations and hope for the
treatment of several infectious diseases. Inappropriate and excess use of antibiotics has
led to the emergence of antibiotic-resistant (AMR) worldwide, which has become one
of the greatest threats to global health. However, in the late 1940s, after approval, mass
production (lead to reduced cost) and supply (lead to easy access to all people) led to
the emergence of Antimicrobial Resistance (AMR). A similar behavioral pattern
ensued as other classes of antibiotics were discovered (through increasing utilization to
resistance). Substandard infection control practices in public healthcare settings eased
the spread and transmission of resistant organisms and intensified antimicrobials'
effect. The healthcare community responded with two major programs – Infection
Control in the 1980s and Antimicrobial Stewardship (in the last decade). These
programs depend on the end-user; however, while the importance of such global
control and prevention programs cannot be disputed, these efforts alone are insufficient
against the advent of AMR. Also, drug discovery has suffered from a shortage of
exploitable bacterial target sites, leading to the slow evolution of novel potent drugs.
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