Carbon dots from Guar Gum: Synthesis, characterization and preliminary in vivo application in plant cells

2019 ◽  
Vol 241 ◽  
pp. 92-99 ◽  
Author(s):  
S.K. Bajpai ◽  
A. D'Souza ◽  
Basharat Suhail
Keyword(s):  
Guar Gum ◽  
2018 ◽  
Vol 15 (3) ◽  
pp. 367-387 ◽  
Author(s):  
Abhinav Sharma ◽  
Bimlesh Kumar ◽  
Sachin Kumar Singh ◽  
Monica Gulati ◽  
Yogyata Vaidya ◽  
...  

2021 ◽  
Author(s):  
Lijuan Liu ◽  
Shengting Zhang ◽  
Xiaodan Zheng ◽  
Hongmei Li ◽  
Qi Chen ◽  
...  

Fusobacterium nucleatum has been employed for the first time to synthesize fluorescent carbon dots which could be applied for the determination of Fe3+ ions in living cells and bioimaging in vitro and in vivo with excellent biocompatibility.


2021 ◽  
Vol 123 ◽  
pp. 112022
Author(s):  
Xiangping Wen ◽  
Guangming Wen ◽  
Wenyan Li ◽  
Zhonghua Zhao ◽  
Xine Duan ◽  
...  
Keyword(s):  

Nanomaterials ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 180
Author(s):  
Maud Weiss ◽  
Jiahui Fan ◽  
Mickaël Claudel ◽  
Luc Lebeau ◽  
Françoise Pons ◽  
...  

With the growth of nanotechnologies, concerns raised regarding the potential adverse effects of nanoparticles (NPs), especially on the respiratory tract. Adverse outcome pathways (AOP) have become recently the subject of intensive studies in order to get a better understanding of the mechanisms of NP toxicity, and hence hopefully predict the health risks associated with NP exposure. Herein, we propose a putative AOP for the lung toxicity of NPs using emerging nanomaterials called carbon dots (CDs), and in vivo and in vitro experimental approaches. We first investigated the effect of a single administration of CDs on mouse airways. We showed that CDs induce an acute lung inflammation and identified airway macrophages as target cells of CDs. Then, we studied the cellular responses induced by CDs in an in vitro model of macrophages. We observed that CDs are internalized by these cells (molecular initial event) and induce a series of key events, including loss of lysosomal integrity and mitochondrial disruption (organelle responses), as well as oxidative stress, inflammasome activation, inflammatory cytokine upregulation and macrophage death (cellular responses). All these effects triggering lung inflammation as tissular response may lead to acute lung injury.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Himanshu Kushwah ◽  
Nidhi Sandal ◽  
Meenakshi Chauhan ◽  
Gaurav Mittal

Abstract Background Uncontrolled bleeding is one of the primary reasons for preventable death in both civilian trauma and military battle field. This study evaluates in vitro and in vivo hemostatic potential of four biopolymeric natural gums, namely, gum tragacanth, guar gum, xanthan gum, and gum acacia. In vitro evaluation of whole blood clotting time and erythrocyte agglutination assay were carried out. In vitro cytotoxicity studies with respect to each gum were done in human lymphocytes to ascertain percent cell viability. In vivo hemostatic potential of each gum (as sponge dressing and powder form) was evaluated in Sprague Dawley rats using tail bleeding assay and compared with commercially available hemostatic sponge. Other important parameters like (a) time taken for complete hemostasis, (b) amount of blood absorbed, (c) adherence strength of developed hemostatic dressing(s), (d) incidence of re-bleeding, and (e) survival of animals were also studied. Results Of the four test gums studied, xanthan gum (@3mg/ml of blood) and gum tragacanth (@35mg/ml of blood) were able to clot blood in least time (58.75±6.408 s and 59.00±2.082 s, respectively) and exhibited very good hemostatic potential in vitro. Except for xanthan gum, all other test gums did not exhibit any significant cytotoxicity at different time points till 24 h. In rat tail bleeding experiments, gum tragacanth sponge dressing and powder achieved hemostasis in least time (156.2±12.86 s and 76±12.55 s, respectively) and much earlier than commercially available product (333.3±38.84 s; p˂0.01). Conclusion Results indicate potential of gum tragacanth to be developed into a suitable hemostatic product.


2003 ◽  
Vol 19 (5) ◽  
pp. 355-362 ◽  
Author(s):  
Y.S.R Krishnaiah ◽  
V Satyanarayana ◽  
B Dinesh Kumar ◽  
R.S Karthikeyan ◽  
P Bhaskar

2016 ◽  
Vol 4 (46) ◽  
pp. 7398-7405 ◽  
Author(s):  
Shanghao Li ◽  
Isaac Skromne ◽  
Zhili Peng ◽  
Julia Dallman ◽  
Abdulrahman O. Al-Youbi ◽  
...  

Accidents, disease and aging compromise the structural and physiological functions of bones, and an in vivo bone imaging test is critical to identify, detect and diagnose bone related development and dysfunctions.


2017 ◽  
Vol 114 (38) ◽  
pp. 10238-10243 ◽  
Author(s):  
Xiaorong Zhang ◽  
G. Paul H. van Heusden ◽  
Paul J. J. Hooykaas

The bacteriumAgrobacterium tumefacienscauses crown gall tumor formation in plants. During infection the bacteria translocate an oncogenic piece of DNA (transferred DNA, T-DNA) into plant cells at the infection site. A number of virulence proteins are cotransported into host cells concomitantly with the T-DNA to effectuate transformation. Using yeast as a model host, we find that one of these proteins, VirD5, localizes to the centromeres/kinetochores in the nucleus of the host cells by its interaction with the conserved protein Spt4. VirD5 promotes chromosomal instability as seen by the high-frequency loss of a minichromosome in yeast. By using both yeast and plant cells with a chromosome that was specifically marked by alacOrepeat, chromosome segregation errors and the appearance of aneuploid cells due to the presence of VirD5 could be visualized in vivo. Thus, VirD5 is a prokaryotic virulence protein that interferes with mitosis.


2021 ◽  
Vol 25 ◽  
pp. 101178
Author(s):  
Chen Dong ◽  
Shuna Wang ◽  
Menghui Ma ◽  
Peifa Wei ◽  
Yan Chen ◽  
...  
Keyword(s):  

2021 ◽  
Author(s):  
Jie Yang ◽  
Shuai Zhou ◽  
Zhengbiao Gu ◽  
Li Cheng ◽  
Chun Cui ◽  
...  

The purpose of this study was to investigate the effect of starch-hydrocolloid (Gum Arabic, Xanthan Gum, and Guar Gum) complexes by heat-moisture treatment (HMT) on in vivo digestibility. In vivo...


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