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Perfluorohexane pfh

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Perfluorohexane (PFH) is a colorless, volatile liquid chemical compound. It has the molecular formula C6F14. PFH is used as a specialty solvent and intermediate in various industrial applications.

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Lab products found in correlation

Distearoyl phosphatidylcholine dspc, by Avanti Polar Lipids (1 mentions) Dulbecco s phosphate buffered saline dpbs, by Cytiva (1 mentions) K3fe cn 6, by Sinopharm (1 mentions)

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Perfluorohexane (4 citations)

2 protocols using perfluorohexane pfh

1

Lipid-Based Nanoparticle Formulation

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Distearoyl phosphatidylcholine (DSPC) was purchased from Avanti Polar Lipids, Inc. (Alabaster, AL) and distearoyl phosphatidylethanolamine-methyl poly(ethylene glycol) MW5000 (mPEG-DSPE 5k) was purchased from Laysan Bio, Inc. (Arab, AL). Dulbecco’s phosphate buffered saline (DPBS) was purchased from Hyclone Laboratories Inc. (Logan, UT). The lipophilic carbocyanine dye, DiI, was purchased from Biotium, Inc. (Hayward, CA). Perfluorohexane (PFH) was purchased from Sigma-Aldrich (St. Louis, MO).
Schutt C.E., Ibsen S.D., Benchimol M.J., Hsu M.J, & Esener S.C. (2014). Manipulating Nanoscale Features on the Surface of Dye-Loaded Microbubbles to Increase their Ultrasound-Modulated Fluorescence Output. Small (Weinheim an der Bergstrasse, Germany), 10(16), 3316-3324.
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2

Synthesis of Hollow Mesoporous Prussian Blue Nanoparticles

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All chemicals were of analytical grade and were used without further purification. Polyvinylpyrrolidone (PVP, K30), potassium ferricyanide (K3 [Fe(CN)6]), hydrochloric acid (HCl, 36.0 %~38.0 %) and perfluorohexane (PFH, Sigma-Aldrich-Co. LLC., St. Louis, MO, US) were purchased from Sinopharm Chemical Reagent Co., Ltd. PVP (3.0 g), K3 [Fe(CN)6] (132 mg) and HCl solution (0.01 M, 40 mL) were mixed under magnetic stirring. After achieving a clear solution, the vial was placed in an electric oven at 80 °C for 24 h. Then, by centrifugation and several washes in distilled water, mesoporous Prussian blue nanoparticles (MPBs) were obtained. PVP (5 mg/mL) was added to the solution of MPBs (1 mg/mL) in a Teflon vessel under magnetic stirring. After 3 h, the solution was placed into a stainless steel autoclave in an electric oven at 140 °C for 4 h. After centrifugation, the precipitates were washed in distilled water several times. HMPBs were acquired after freeze-drying.
Zhang N., Cai X., Gao W., Wang R., Xu C., Yao Y., Hao L., Sheng D., Chen H., Wang Z, & Zheng Y. (2016). A Multifunctional Theranostic Nanoagent for Dual-Mode Image-Guided HIFU/Chemo- Synergistic Cancer Therapy. Theranostics, 6(3), 404-417.
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