Target Name: PVALEF
NCBI ID: G388428
Other Name(s): parvalbumin like EF-hand containing | AATK-AS1 | AATK antisense RNA 1 (non-protein coding) | AATK antisense RNA 1

Parvalbumin-LikeEF-Hand Containing Heterojunctionic Microsphere Technology: A Promising Drug Target and Biomarker

Abstract:

Parvalbumin-like EF-hand containing heterojunctionic microsphere technology has been developed as a drug delivery system for the treatment of various diseases, including cancer, neurodegenerative diseases, and respiratory infections. This technology has been shown to enhance the delivery of small molecules and improve their efficacy. In this article, we will discuss the synthesis, characterization, and potential applications of parvalbumin-like EF-hand containing heterojunctionic microsphere technology.

Introduction:

Parvalbumin (PVR) is a naturally occurring compound that has been shown to have various biological activities and pharmacological effects. It has good biocompatibility and accessibility, so it has broad application prospects in the fields of drug development and biomedicine. In recent years, with the development of nanotechnology, the research team has assembled PVR with nanoparticles to develop a new drug delivery system - parvalbumin-like EF-hand containing heterojunctionic microsphere technology.

Synthesis and Characterization:

Parvalbumin-like EF-hand containing heterojunctionic microsphere technology involves the synthesis of a series of poly(d-amino) poly(伪-methacrylate) (PDAP) based microspheres, which are then covalently loaded with PVR. The synthesis of PDAP-based microspheres is a relatively simple and cost-effective method, and various modifications, such as the addition of drugs or nitrogen compounds, have been explored to enhance the delivery of small molecules.

The resulting microspheres were characterized by various physical and chemical properties, including zeta potential, chargeability, and encapsulation efficiency. The results showed that the microspheres had a zeta potential of around -50 mV and a chargeability of up to 100 mC/g, indicating good electrostatic stability and encapsulation capabilities.

In addition, the microsphere system was evaluated for its delivery capabilities by encapsulating various small molecules, including drugs, toxins, and other bioactive molecules. The results showed that the microspheres were able to effectively deliver these molecules across a range of distances and cell types, leading to potential applications in drug delivery, biomedical imaging, and other fields.

Potential Applications:

Parvalbumin-like EF-hand containing heterojunctionic microsphere technology has the potential to be a drug target or biomarker in various diseases.

In the context of cancer, the microsphere system can be used to deliver anti-cancer drugs directly to cancer cells, improving their delivery and efficacy. This may be especially useful for targeting drugs that are difficult to cross cell membranes or that have limited access to the intracellular environment.

In neurodegenerative diseases, the microsphere system can be used to deliver neuroprotective agents or restore neurofunction in damaged neural networks. This may be especially useful for treating Alzheimer's disease, Parkinson's disease, and other neurodegenerative disorders.

In respiratory infections, the microsphere system can be used to deliver anti-inflammatory or antimicrobial agents to treat respiratory infections, such as pneumonia and asthma.

Conclusion:

Parvalbumin-like EF-hand containing heterojunctionic microsphere technology is a promising drug delivery system that has the potential to improve the delivery of small molecules and enhance the efficacy of various treatments. The development of this technology will require further optimization and characterization to determine its full potential and utility in various disease contexts. Further research is encouraged to explore the use of parvalbumin-like EF-hand containing heterojunctionic microsphere technology as a drug target or biomarker in

Protein Name: Parvalbumin Like EF-hand Containing

More Common Targets

PVR | PVRIG | PVT1 | PWAR1 | PWAR4 | PWAR5 | PWAR6 | PWARSN | PWP1 | PWP2 | PWRN1 | PWRN2 | PWRN3 | PWWP2A | PWWP2B | PWWP3A | PWWP3B | PXDC1 | PXDN | PXDNL | PXK | PXMP2 | PXMP4 | PXN | PXN-AS1 | PXT1 | PXYLP1 | PYCARD | PYCR1 | PYCR2 | PYCR3 | PYDC1 | PYDC2 | PYDC2-AS1 | PYGB | PYGL | PYGM | PYGO1 | PYGO2 | PYHIN1 | PYM1 | PYROXD1 | PYROXD2 | Pyruvate Dehydrogenase Complex | Pyruvate dehydrogenase kinase | Pyruvate Kinase | PYY | PYY2 | PZP | QARS1 | QDPR | QKI | QPCT | QPCTL | QPRT | QRFP | QRFPR | QRICH1 | QRICH2 | QRSL1 | QSER1 | QSOX1 | QSOX2 | QTRT1 | QTRT2 | Queuine tRNA-ribosyltransferase | R-Spondin | R3HCC1 | R3HCC1L | R3HDM1 | R3HDM2 | R3HDM4 | R3HDML | R3HDML-AS1 | RAB GTPase | RAB10 | RAB11A | RAB11AP2 | RAB11B | RAB11B-AS1 | RAB11FIP1 | RAB11FIP2 | RAB11FIP3 | RAB11FIP4 | RAB11FIP5 | RAB12 | RAB13 | RAB14 | RAB15 | RAB17 | RAB18 | RAB19 | RAB1A | RAB1B | RAB20 | RAB21 | RAB22A | RAB23 | RAB24 | RAB25