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Emla 5 cream

Manufactured by AstraZeneca
Sourced in United Kingdom

Emla 5% cream is a topical anesthetic product containing lidocaine and prilocaine as active ingredients. It is used to numb the skin before procedures or treatments. The cream is applied to the skin and allowed to take effect before the intended procedure.

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11 protocols using emla 5 cream

1

Serum Biomarker Evaluation in Rabbits

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Approximately 30 min before dosing, Emla 5% cream (AstraZeneca) was applied to the skin covering the marginal vein of an ear, and the ear was warmed via gentle stroking. After 5 min, a small incision was made across the vein with a sterile scalpel blade, and 1 mL of blood (pretreatment sample) was collected into a sterile vacutainer (BD vacutainers, Franklin Lakes, NJ, USA) containing a clot activator (silicone-coated plastic for serum separation). Rabbits scheduled to be euthanised at 96 h were blood-sampled (post-treatment) again at 48 h.
Immediately following euthanasia (pentobarbitone injected into the marginal ear vein of the ear) or as soon as possible after death, all rabbits were blood sampled (terminal) via cardiac puncture into sterile vacutainers containing a clot activator for serum separation.
The serum was processed for biochemistry at the IDEXX-New Zealand Veterinary Pathology laboratory, Palmerston North, NZ, for the following biomarkers: aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), gamma glutamyltransferase (GGT), glutamate dehydrogenase (GDH), bilirubin, total bile acids, creatinine, amylase, lipase and creatine kinase (CK).
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2

Muscle Biopsy Procedure for Exercise Studies

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Muscle samples were obtained from the right vastus lateralis (VL) of each participant at 7 – 10 days before the first exercise session to allow for adequate tissue recovery after the biopsy procedure, and 5 days after the last exercise session to minimize the effects of potential swelling on the DEXA and ultrasound scanning outcomes. Local anesthetic cream (Emla 5% Cream, AstraZeneca, UK) was applied around the sample site 40 min before taking the muscle biopsy. The pre-training biopsy sample was taken at 50% distance between the greater trochanter and lateral epicondyle using a disposable, spring-loaded microbiopsy system (14g × 10cm, MAX-CORE, Bard Biopsy Systems, USA). The post-training sample was taken 2 cm adjacent to the first one, randomly selected between participants to be either more proximal or distal. From each site, three or four muscle samples were extracted for a total of at least 50 mg of tissue. The tissue samples were frozen immediately in liquid nitrogen and stored at −80°C for later analyses.
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3

Penile Filler Injection Procedure

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At each institution, an experienced physician performed the injection procedure. The detailed procedure has been described previously [8 ]. In summary, the procedure was performed via local anesthesia by injecting lidocaine (Lidocaine HCL Hydrate Injection 2%; Huons, Co., Ltd., Sungnam, Korea) or applying EMLA cream (Emla 5% cream; AstraZeneca Korea, Co., Ltd., Korea). The 17-gauge or 21-gauge injection needle was indwelled on the penile base at the 1–2 o’clock and 10–11 o’clock points. The filler was injected between the dartos and Buck’s fascia using a fanning technique. If necessary, a multiple puncture technique was used at the 3–4 o’clock or 8–9 o’clock points. The injected volume was initially set at 10 to 22 mL, and the actual injection volume was determined according to the penile size and physicians’ experience. After the injection was performed, the patients applied an elastic penile support bandage for 1 day and used antibiotics (first-generation cephalosporin) and non-steroidal anti-inflammatory drugs (NSAIDs) for 3 days. Patients were instructed to massage the penile shaft gently and to abstain from sexual intercourse for 1 month.
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4

Rabbit Euthanasia and Blood/Liver Collection

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The experiment lasted for 21 d, and 30 rabbits (6 rabbits in each group were randomly selected) were euthanized after fasting for 24 h after the last feeding (n = 6). Blood and liver samples were collected. Part of the liver samples was fixed in 4% paraformaldehyde, and the rest were immediately stored at −80 °C for further experiments. We applied Emla 5% cream (AstraZeneca, Cambridge, UK) to the skin covering the vein at the edge of the ear about 5 min before the rabbit was euthanized and warmed the ear by gentle stroking. Five minutes later, pentobarbital was slowly injected into the marginal auricular vein of rabbits at a dose of 100 mg/kg. All animal care and handling were carried out in adherence to institutional and national guidelines.
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5

Penile Filler Injection Technique

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The injection technique for PGE has been described in detail earlier [12 (link)]. Briefly, under local anesthesia with the application of EMLA cream (EMLA 5% cream; AstraZeneca Korea, Co., Ltd., Korea) or penile dorsal nerve block, patients were placed in the supine position, and a medical curtain was placed at the umbilical level for a patient-blinded procedure. Entry sites were made using 21-gauge or 18-gauge needles for the HA or PLA filler, respectively. Four entry sites were made on the penile base and distal penile shaft at the 2 o'clock and 10 o'clock positions, respectively. Subsequently, using a 22-gauge or 20-gauge cannula, HA or PLA filler was injected in the respective group of patients, between the Buck's fascia and the dartos fascia, by combining the back-and-forth and fanning techniques. Depending on the penile size, 15–22 mL of HA or PLA filler was injected. After the procedure, a mild compressive dressing was applied to the penis and left in place overnight. Patients were advised to abstain from sexual intercourse for 4 weeks after the procedure.
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6

Radiesse Injection Technique Comparison

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A topical anesthetic (EMLA® 5% cream; AstraZeneca AB, Sweden) was applied to the hands of each participant, 20 minutes before injection. With their vision obscured, participants were injected in one hand (N hand) with 0.8 mL Radiesse® mixed with 0.2 mL 2% lidocaine solution using uniform multipoint needle (27 G) injections [Figure 2a]. In the other hand (C hand), injections were performed using a blunt cannula (25 G; 50 mm) in the upper subdermal layer (depth of 2-3 mm) in a fan-like distribution [Figure 2b]. Following each injection, hands were massaged.
At Month 3, additional touch-up injections could be performed according to participants’ wishes using the same procedures as described previously.
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7

Topical Anesthetic for Acupuncture Procedure

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Emla cream 5% (lidocaine 25 mg/g, prilocaine 25 mg/g; Astrazeneca Korea, Seoul, Republic of Korea) was used as an anesthetic. A 30 G × 1/2 needle manufactured by the International Hongchim Association connected to an 80 mm folder was used for Jae-Seng Acupuncture treatment.
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8

Maintenance of Portal Access for Cell Infusion

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Patency of the VAP system was checked by flushing portal and catheter with saline once daily on the first 2 days after surgery before and after infusing cells through the VAP into the portal bloodstream. Images of the portal vein and the tip of the catheter were obtained by B-mode imaging and colour Doppler was applied to check for hepatopetal flow during infusion. The gripper needle was removed 5 days after surgery.
Subsequently, patency was checked by flushing the VAP system once a month. The skin overlying the portal was clipped, locally anesthetized with a combined lidocaine and prilocaine ointment EMLA Cream 5% (AstraZeneca, Den Haag, The Netherlands) and routinely disinfected. A 19G gripper needle (reference number: 21–3468-24, Smiths Medical Nederland B.V) was inserted percutaneously into the subcutaneous portal. Using a syringe, 5 ml of blood was withdrawn and the catheter was subsequently flushed with 10 ml of saline. Patency of the portal vein and the position of the intravenous catheter were also checked with abdominal ultrasonography. After each use of the VAP, a heparin lock was placed by infusion of 5 ml of heparinized saline (100 IU/ml).
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9

Subcutaneous RFID Microchip Implantation in Mice

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Radio frequency identification microchips were injected subcutaneously into the lower left or right quadrant of the abdomen of each mouse at 12 weeks of age for the C57BL/6J study and 7 weeks of age for the B6-TgN(HD82Gln)81Dbo/H study. These microchips were contained in standard ISO-biocompatible glass capsules (11.5 × 2 mm; PeddyMark Ltd., UK). The procedure was performed on sedated mice (Isoflo; Abbott, UK) after topical application of local anesthetic cream on the injection site prior to the procedure (EMLA Cream 5%; AstraZeneca, UK) as described in Hobson et al. (2020 (link)). The animals were allowed to recover from the microchip procedure for at least 1 week before being placed in the HCA rigs for data collection. The procedure for data collection has been described previously in Bains et al. (2016 (link)) and Hobson et al. (2020 (link)), briefly, microchipped animals were placed in the HCA rigs for 72 h of continuous recording for every age group. At the end of the 72-h recording period for that age, the animals in their IVCs were returned to the standard IVC rack, until the animals reached the next age group to be recorded, where the procedure was repeated for another 72 h.
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10

Punch Biopsy Wound Healing Assay

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Analgesic EMLA cream 5% (AstraZeneca) was applied to the skin for 10 min before mice were anaesthetised using isoflurane (Cp-pharma). A 2 mm diameter punch biopsy (Stiefel) was used to make a full-thickness wound in the central back skin or tail base at the indicated time points. If necessary, the hair on the back was clipped prior to wounding. When neonatal mice (P2-P10) were wounded, all litter pups were wounded and housed with their mother until weaning age. Wound closure was quantitated by comparing digital wound bed photos taken at different times after wounding.
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