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Oxytetracycline hcl

Manufactured by Merck Group
Sourced in United States

Oxytetracycline HCl is a chemical compound used in laboratory settings. It is a crystalline powder that serves as a versatile reagent for various analytical and experimental applications.

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4 protocols using oxytetracycline hcl

1

Tetracycline Antibiotic Formulations and Dosing

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Ethanol (95% v/v, USP) was diluted to 20% (v/v) with rodent drinking water from the Laboratory Animal Resources Center, Texas Tech University Health Sciences Center, Lubbock TX. Tetracycline derivatives and their properties are listed in Table 1. All tetracyclines used in our study have been approved by the FDA as antibiotics in doses varying up to 500 mg, although some are no longer used (see: http://www.accessdata.fda.gov/scripts/cder/drugsatfda/). Drugs were obtained from commercial sources and stored according to the vendor's recommendations. Minocycline HCl (#M9511), chlortetracycline HCl (#46133-Fluka), oxytetracycline HCl (# D9811), tigecycline hydrate (#PZ0021), and tetracycline HCl (#T3383) were obtained from Sigma-Aldrich (St. Louis, MO, USA). Doxycycline HCl (#SC337691) and demeclocycline HCl (#SC204710A) were obtained from Santa Cruz Biotechnology (Dallas, TX, USA) and tigecycline (base) (#15026) was obtained from Cayman Chemical (Ann Arbor, MI, USA). Doses of 0, 20, 40, 60, 80, 100 and 120 mg/kg were made fresh and used within 25 hours.
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2

Fluorescent Bone Marker Dynamics

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During the 12 weeks healing period, fluorescent bone markers were injected 55 (link) to observe the dynamics of new bone formation. Three weeks after the operation, 20 mg alizarin red S/kg of body weight was administered intraperitoneally (IP) (Sigma-Aldrich), 20 mg oxytetracycline HCl/kg of body weight (Sigma-Aldrich) was injected IP at 6 weeks post-surgery, and 20 mg xylenol/kg of body weight (Sigma-Aldrich) was injected IP at 9 weeks post-surgery. All dyes were prepared immediately before use in saline.
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3

Visualizing Bone Remodeling Dynamics

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After 8 weeks of healing, the dynamics of the newly formed bones were observed by injecting them with fluorescent bone marker labels. At 2 weeks, alizarin red S (20 mg/kg body weight), oxytetracycline HCl (20 mg/kg body weight), and xylenol (20 mg/kg body weight) (Sigma-Aldrich) were administered via intraperitoneal injection. All dyes were prepared with saline immediately before use. To visualize remodeled bone, an intravital multiphoton microscope (SP8-MP; Leica, Wetzlar, Germany) with a water immersion lens (25×, 0.9 NA) was used. The fluorophores were excited using the InSight DS Plus laser system (Spectra-Physics, Santa Clara, USA) at the following wavelengths: xylenol (excitation = 800 nm, emission = 375-570 nm), oxytetracycline (excitation = 1040 nm, emission = 365-490 nm), and alizarin (excitation = 1180 nm, emission = 538-580 nm). Alizarin -, oxytetracycline-, and xylenol-positive areas were quantified using the ImageJ software. All values are expressed as mean ± SD (n = 4).
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4

Synthesis of Polymeric Adsorbent Materials

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Oxytetracycline HCl ( 95%), 2-acrylamido-2-methylpropane sulfonic acid (AMPS) and ethylene glycol dimethacrylate (EGDMA) were from Sigma-Aldrich (St. Louis, Mo, USA); 1,1´-azobis(isobutyronitrile) (AIBN) from Acros (Geel, Belgium); 2hydroxyethyl methacrylate (HEMA) and hydrochloric acid from Merck (Darmstadt, Germany); dimethylsulfoxide (DMSO) from Scharlau Chemicals (Barcelona, Spain); methanol HPLC gradient from Prolabo (Barcelona, Spain); and sodium chloride (NaCl) from Panreac (Barcelona, Spain). Purified water was obtained by reverse osmosis (MilliQ®, Millipore).
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