PAL resin
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PAL resin

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

PAL resin is useful for the synthesis of peptide amides using Fmoc strategy. Cleavage has been performed with 50% TFA in CH2Cl2 or 95% aqueous TFA. Scavengers may be required.

Category
Other Resins
Catalog number
BAT-014451
Synonyms
H2NCH2-Ph(OCH3)2-O-CH2-polymer; 4-Alkoxy-2,6-dimethoxybenzylamine resin
Appearance
Yellow-brown Resin
DVB Crosslinking
1% DVB
Mesh Size
200-400 mesh
Substitution
0.2-0.5 mmol/g
Storage
Store at 2-8°C
1. Phytocatalytic and cytotoxic activity of the purified laccase from bled resin of Pistacia atlantica Desf
Azam ElyasiGhahfarokhi, Saba Hashemi, Mina Saeedi, Mahnaz Khanavi, Mohammad Ali Faramarzi Int J Biol Macromol. 2021 Apr 15;176:394-403. doi: 10.1016/j.ijbiomac.2021.01.212. Epub 2021 Feb 3.
This study reports an efficient and fast procedure for the purification of laccase (PaL) obtained from the resin of Pistacia atlantica Desf. It was purified by one-step affinity chromatography and showed the specific activity of 393 U/mg with 81.9-fold purification. The molecular weight of PaL was estimated to be approximately 60 kDa using gel electrophoresis SDS-PAGE. Moreover, it depicted diphenolase activity and high affinity towards 2,6-dimethoxy phenol (Km = 10.01 ± 0.5 mM) and syringaldazine (Km = 6.57 ± 0.2 mM) comparing with plant-origin polyphenol oxidases reported in the literature. It should be noted that PaL possessed optimal activity at pH 7.5 and 45 °C. It also remained stable under different conditions of pH (6.5-8.0), temperature (25-45 °C), and when it was exposed to several metal ions. The MTT and flow cytometry assays demonstrated that the enzyme treatment significantly affected growth of HeLa, HepG2, and MDA-MB-231 cells with LC50 values of 4.83 ± 0.02, 61 ± 0.31, and 26.83 ± 0.11 μM after 72 h, respectively. NOVELTY STATEMENT: This is the first attempt to isolate and characterize a new oxidoreductase from the resin of Pistacia atlantica Desf., native species of Iran, to recruit it in cytotoxicity researches. In the purification process by an efficient affinity column (SBA-NH2-GA), the enzyme was eluted promptly with a satisfied yield. The purified laccase exerted higher affinity to diphenolic compounds and pH-thermal stability compared to other plant-derived polyphenol oxidases. The purified enzyme was found to show anti-oxidant capacity and significantly inhibited the growth of cancerous cells in vitro. PaL showed more cytotoxic activity towards HeLa and MDA-MB-231 cells by induction of apoptosis. The cytotoxic activity of the laccase was measured by flow cytometry.
2. Benzodioxole derivative as coinitiator for dental resin
Shiji Liu, Suqing Shi, Guangyu Hou, Jun Nie Acta Odontol Scand. 2007 Nov;65(6):313-8. doi: 10.1080/00016350701742349.
Objective: The aim of this work was to examine whether it was possible to substitute benzodioxole derivatives for amine as coinitiators for dental application. Material and methods: A mixture of urethane dimethacrylate (UDMA)/triethylene glycol dimethacrylate (TEGDMA) (70/30 wt%), camphorquinone (CQ) and coinitiators was photocured. Real time Fourier Transform Infrared Spectroscopy with a horizontal sample holder was used to monitor the extent of polymerization. Dynamic mechanical analysis was performed over a temperature range from -50 degrees C to 200(o)C, with a ramping rate of 5(o)C per minute, using extension mode. Results: Benzodioxole derivatives as coinitiator improved the rate of polymerization and final double bond conversion of the dental resin. The cured samples showed similar properties, e.g. modulus, glass transition temperature, water sorption and solubility. Conclusion: The results indicate that two benzodioxole derivatives, piperonyl alcohol (PAL) and benzodioxole (BDO), are viable alternatives to conventional amines as coinitiator. The biocompatibility of benzodioxole derivatives makes them more promising than amine in dental resin formulations.
3. Radiation-induced dental caries, prevention and treatment - A systematic review
Nishtha Gupta, et al. Natl J Maxillofac Surg. 2015 Jul-Dec;6(2):160-6. doi: 10.4103/0975-5950.183870.
Treatment of head and neck cancers (HNCs) involves radiotherapy. Patients undergoing radiotherapy for HNCs are prone to dental complications. Radiotherapy to the head and neck region causes xerostomia and salivary gland dysfunction which dramatically increases the risk of dental caries and its sequelae. Radiation therapy (RT) also affects the dental hard tissues increasing their susceptibility to demineralization following RT. Postradiation caries is a rapidly progressing and highly destructive type of dental caries. Radiation-related caries and other dental hard tissue changes can appear within the first 3 months following RT. Hence, every effort should be focused on prevention to manage patients with severe caries. This can be accomplished through good preoperative dental treatment, frequent dental evaluation and treatment after RT (with the exception of extractions), and consistent home care that includes self-applied fluoride. Restorative management of radiation caries can be challenging. The restorative dentist must consider the altered dental substrate and a hostile oral environment when selecting restorative materials. Radiation-induced changes in enamel and dentine may compromise bonding of adhesive materials. Consequently, glass ionomer cements have proved to be a better alternative to composite resins in irradiated patients. Counseling of patients before and after radiotherapy can be done to make them aware of the complications of radiotherapy and thus can help in preventing them.
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